Estrogen nucleus derivatives for use in the inhibition of sex steroid activity

ABSTRACT

Novel derivatives of estrogenic nuclei, contain a side-chain substitution of the formula --R 1   B--R 2  --! x  L--G and may be used in pharmaceutical compositions as sex steroid activity inhibitors useful in the treatment of both androgen-related and estrogen-related diseases.

RELATED APPLICATIONS

This application is a division of application Ser. No. 08/017,045, filed Feb. 12, 1993, now U.S. Pat. No. 5,631,249, which is in turn a division of application Ser. No. 917,915 filed Jul. 21, 1992 now U.S. Pat. No. 5,204,337, which is in turn a continuation of application Ser. No. 07/377,010 filed Jul. 7, 1985, abandoned, which is in turn continuation-in-part of U.S. patent application Ser. No. 07/322,154 filed Mar. 10, 1989, now abandoned, and of U.S. application Ser. No. 07/265,716 filed Nov. 1, 1988, now abandoned, and of U.S. application Ser. No. 07/265,150 filed Oct. 31, 1988, now abandoned, the disclosures of which are incorporated herein by reference.

BACKGROUND OF THE INVENTION

This invention relates to novel inhibitors of sex steroid activity such as antiestrogen compounds having effective antagonistic capability while substantially lacking agonistic effects. More particularly, certain preferred embodiments of the invention relate to certain estradiol and non-steroidal diphenylethylene analogs which have high affinity for estrogen receptors but do not activate such receptors and/or which inhibit the production of sex steroids or their precursors.

During the treatment of certain sex steroid-dependent diseases, it is important to greatly reduce or, if possible, eliminate certain sex steroid-induced effects. For this purpose, it is desirable both to block receptor sites stimulated by sex steroids and also to reduce the amount of sex steroid available to act at these sites. For example, alternative or concurrent therapy to administration of antiestrogens could involve attempts to block the production of estrogens (e.g. by ovariectomy) such that less is available to activate receptor sites. However, prior art methods for blocking estrogen production insufficiently inhibit estrogen-induced functions. Moreover, it is possible that even in the total absence of sex steroids, unoccupied sex steroid receptors may be biologically active. Hence, antagonists of sex steroids may produce greater therapeutic results than therapy which only inhibits sex steroid production. Prior art antagonists, however, often have insufficient affinity for receptors, and some, although capable of binding the receptors, may themselves act as agonists and undesirably activate some receptors and induce the same effects as a sex steroid.

There is, therefore, a need in the art for antiestrogens which effectively block estrogen receptors with minimal or no agonistic effect. Numerous compounds have been tried in the art with mixed results. Known antiestrogens continue to exhibit undesirable agonistic activity. See, for instance, Wakeling and Bowler, "Steroidal Pure Antioestrogens", J. Endocrinol. (1987) 112, R7-R10. The net effectiveness of prior art compounds is determined by the balance between their agonistic and antagonistic activities. Certain steroidal derivatives similar to those disclosed in the foregoing article, and which are stated to have antioestrogenic effect, are set forth in Bowler et al., U.S. Pat. No. 4,659,516.

In U.S. Pat. No. 4,094,994, it is disclosed that the use of certain antiestrogens may inhibit certain human breast tumor cells.

H. Mooridsen et al., Cancer Treatment Review 5, 131-141, (1978), discloses that Tamoxiphen, an antiestrogen, is effective in remission of advanced breast cancer in about 30 percent of the women patients treated.

The combined use of the antiestrogen Tamoxiphen and a luteinizing hormone-releasing hormone agonist, Buserelin, is also known for treatment of breast cancer. See, for instance, Klijn et al., J. Steroid Biochem, 420, No. 6b, 1381 (1984); The objective remission of such cancers, however, remains unacceptably low.

It has been found that certain 7α-substituted derivatives of estradiol possess antiestrogenic activity (Bowler et al., 1985; Eur. Patent Application 0138504; Wakeling and Bowler, J. Steroid Biochem. 30: 141-147, 1988).

In U.S. Pat. No. 4,659,516, Bowler et al. report antiestrogenic activity for certain 7α substituted derivatives of estradiol.

For a number of years, there has been research for compounds which can efficiently inhibit androgen and/or estrogen formation (e.g. enzyme inhibitors) or for compounds which may suppress androgen or estrogen action (steroid antagonists), without causing adverse effects to healthy tissues.

Recently, estradiol derivatives bearing a carboxyalkyl substituent at the 7α-position maintained their affinity for the estrogen receptor when linked via their carboxy group to agarose or polyacrylamide resin for affinity chromatography purification of the estrogen receptor (Bucourt et al., J. Biol. Chem. 253: 8221, 1978).

Non steroidal compounds bearing a similar aliphatic side chain have also been found to possess antiestrogenic activity (U.S. Pat. No. 4,732,912).

Some steroid derivatives, such as especially 16-methylene estradiol and 16-methylene estrone, have been described as inhibitors of 17β-hydroxysteroid dehydrogenase activity (Thomas et al., J. Biol. Chem. 258: 11500, 1983).

Prior art methods have not been completely effective in inhibiting sex steroid synthesis while avoiding undesirable side effects.

Certain nonsteroidal compounds which are stated to have antiandrogenic effect are described by Furr et al., J. Endocr. 113, R7-R9, 1987.

In U.S. Pat. No. 4,659,695 relates to a method of treatment of prostate cancer for susceptible male animals including humans whose testicular hormonal secretions are blocked by surgical or chemical means, e.g., by use of an LHRH agonist, e.g., D-Trp⁶, des-Gly-NH₂ ¹⁰ !LHRH ethylamide. The treatment includes administering an antiandrogen, e.g., flutamide in association with at least one inhibitor of sex steroid biosynthesis, e.g., aminoglutethimide and/or ketoconazole.

U.S. Pat. No. 4,472,382 relates to a method of treating prostate cancer using the combination of an antiandrogen and an LHRH agonist.

In U.S. Pat. No. 4,386,080 relates to new amide derivatives, and more particularly novel acylanilides, possess antiandrogenic properties.

In French, Patent 2528434 and in Jordan and Koch, "Regulation of Prolactin Synthesis in vitro by estrogenic and antiestrogenic derivatives of estradiol and Estrone", Endocrinology 124(4): 1717-1725 (1989), antiestrogenic effects are described for certain 11β-long chain substituted estradiol derivatives.

In U.S. Pat. No. 3,995,060, U.S. Pat. No. 4,161,540 and U.S. Pat. No. 4,139,638, it is disclosed that certain 4'-substituted and 3'-, 4'-disubstituted anilides have antiandrogenic properties.

EP Pat. No. 138 504, EP Pat. No. 166 509, EP Pat No. 124 369, EP Pat. No. 160 508, EP Pat. No. 163 416, U.S. Pat. No. 4,732,912, U.S. Pat. No. 4,760,061, U.S. Pat. No. 4,751,240, U.S. Pat. No. 4,659,516 and Wakeling A. E. and Bowler J., J. Endocr. 112, R7-R10, 1987, and J. Steroid Biochem. 30, 141-147, 1988 disclose that certain long chain substitutions onto an estrogenic nucleus may result in compositions exhibiting antiestrogenic activity.

For a number of years, there has been search for compounds which can efficiently inhibit androgen and/or estrogen formation without causing adverse effects to healthy tissues. More particularly, the inhibition of 17β-hydroxysteroid dehydrogenase, which is involved in the biosynthesis of testosterone, androst-5-ene-3β,17β-diol and estradiol, has been studied by some workers. Some affinity-label inhibitors for human placental estradiol 17β-dehydrogenase have been described (C. C. Chin and J. C. Warren, J. Biol. Chem. 250, 7682-7686, 1975; Y. M. Bhatnagar et al., J. Biol. Chem. 253, 811-815, 1978; C. C. Chin et al., J. Biol. Chem. 255, 3660-3664, 1980; J. L. Thomas and R. C. Strickler, J. Biol. Chem. 258, 1587-1590, 1983).

B. Tobias et al., J. Biol. Chem. 257, 2783-2786, 1982 and R. J. Auchus and D. F. Covey, Biochemistry 25, 7295-7300, 1986 disclose, respectively, the use of 17β-propynyl-substituted progestins and propynyl-substituted 3-hydroxy-14,15-secoestra-1,3,5(10)-trien-17-one as inhibitors of the 17β-estradiol dehydrogenase.

Thomas J. L. et al., J. Biol. Chem. 258, 11500, 1983 have described that 16-methylene estradiol and 16-methylene estrone are inhibitors of 17β-hydroxysteroid dehydrogenase activity.

OBJECTS OF THE INVENTION

It is an object of the present invention to provide methods of inhibiting sex steroid activity. Such methods may be useful in the treatment of sex steroid-related diseases.

It is another object of the invention to provide a steroidal pure antiestrogen for therapeutic use.

It is another object of the invention to provide compositions capable of inhibiting sex steroid synthesis, especially estrogen synthesis.

It is another object to provide an antiestrogen having good affinity for estrogen receptors, but substantially lacking undesirable agonistic activity regarding these receptors and substantially lacking hormonal activity.

It is another object of the invention to provide a therapeutic antiestrogenic composition useful in the treatment of estrogen-related diseases. These diseases include, but are not limited to, breast cancer, uterine cancer, ovarian cancer, endometriosis, uterine fibroma, precocious puberty and benign prostatic hyperplasia.

It is another object of the invention to provide inhibitors of sex steroid production useful in the treatment of both estrogen- and androgen-related diseases. Androgen-related diseases include but are not limited to prostate cancer, ache vulgaris, hirsutism, precocious puberty, benign prostatic hyperplasia, seborrhea, androgenic alopecia and sexual deviants. Control of androgen activity may also be useful in male contraception.

SUMMARY OF THE INVENTION

The present invention provides a method of inhibiting sex steroid activity in a warm-blooded animal, including humans, comprising administering to said animal a therapeutically effective amount of a compound having as part of its molecular structure an estrogenic nucleus of general structure I: ##STR1## wherein the dotted lines represent optional pi bonds and wherein said compound includes as another part of its molecular structure a side chain substituents onto a ring carbon of said general structure I represented by the formula --R¹ --B--R² --!_(x) L--G wherein at least one of said side chains is substituted at a ring carbon selected from the group consisting of carbon 14, carbon 15, carbon 16 and carbon 17, wherein:

x is an integer from 0 to 6, wherein at least one of L and G is a polar moiety distanced from said ring carbon by at least three intervening atoms, and wherein:

R¹ and R² are independently either absent or selected from the group consisting of straight- or branched-chain alkylene, straight- or branched-chain alkynylene, straight- or branched-chain alkenylene, phenylene, and fluoro-substituted analogs of the foregoing;

B is either absent or selected from the group consisting of --O--, --S--, --Se--, --SO--, --SO₂ --, --NR³ --, --SiR³ ₂ --, --CR³ OR³ --, --NR³ CO--, --NR³ CS--, --CONR³ --, --CSNR³ --, --COO--, --COS--, --SCO--, --CSS--, --SCS--, --OCO-- and phenylene (R³ being hydrogen or lower alkyl);

L is either a moiety which together with G, forms a heterocyclic ring having at least one nitrogen atom or is selected from the group consisting of lower alkyl, --CONR⁴ --, --CSNR⁴ --, --NR⁵ CO--, --NR⁵ CS--, --NR⁵ CONR⁴ -- ##STR2## --SO₂ NR⁴ --, --CSS--, --SOS--, --(NO)R⁴ --, --(PO)R⁴ --, --NR⁵ COO--, --NR⁵ SO₂ --, --O--, --NR⁴ --, --S--, --SO-- and --SO₂ -- (R⁴ and R⁵ being independently selected from the group consisting of hydrogen and lower alkyl; and R⁶ being selected from the group consisting of hydrogen, nitrile and nitro); and

G is either a moiety which together with L forms a heterocyclic ring having at least one nitrogen atom, or is selected from the group consisting of hydrogen, lower alkyl, lower alkenyl, lower alkynyl, (C₃ -C₇)cycloalkyl, bromo(lower)alkyl, chloro(lower)alkyl, fluoro(lower)alkyl, iodo(lower)alkyl, cyano(lower)alkyl, carboxy(lower)alkyl, (lower)alkoxycarbonyl(lower)alkyl, (C₆ --C₁₀) aryl, (C₇ -C₁₁) arylalkyl, di(lower)alkylamino(lower)alkyl and fluoro-substituted analogs of the foregoing.

The invention further provides a method of inhibiting sex steroid activity in a warm-blooded animal, including humans, comprising administering a therapeutically effective mount of at least one compound having, as part of its molecular structure, a substituted or unsubstituted estrogenic nucleus of general structure I: ##STR3## wherein the dotted lines represent optional pi bonds; and wherein said compound includes as another part of its molecular structure a side chain substitution onto a ring carbon of said general structure I in at least one position selected from the group consisting of 7, 11, 14, 15, 16, 17, (preferably 7α, 15α, or 17α), a side chain of the formula --R¹ --B--R² --!_(x) L--G, as defined above, and wherein general structure I further includes at least one substitution selected from the group consisting of 15-halo, 16-halo, 14-hydroxyl, 15-hydroxyl, 14-lower alkyl, 15-lower alkyl (and halogenated or cyano derivatives of foregoing), 14-nitro, 15-nitro, 16-nitro-, 14-alkoxy, 15-alkoxy, 16-alkoxy, 14-alkyl (or dialkyl) amino, 15-alkyl (or dialkyl) amino, 16-alkyl (or dialkyl) amino, 14-cyano, 15-cyano, 16-cyano, a 15,16 bridge atom (preferably carbon) a 14,15 bridge atom (preferably oxygen), 16-pi-bonded lower alkyl and 16-pi-bonded lower halogenated alkyl.

Chloro- or bromo-substitution at the 16 position is preferred. A pi-bonded lower alkyl substitution at 16 is believed to increase efficacy of compounds utilized in the foregoing methods, as is an alkynyl substitution at the 17α position. In preferred embodiments R¹⁷ is hydroxyl or in some embodiments R¹⁷α and R¹⁷β together are=0.

The present invention further provides methods for the treatment of sex steroid-related diseases by administering therapeutically effective amounts of sex-steroid activity inhibitors as disclosed herein (with or without pharmaceutical carriers or diluents). Sex steroid-related diseases include any disease whose onset, maintenance or progress is, at least in part, dependent upon biological activities induced by sex steroids such as androgens and estrogens. For example, androgen-dependent diseases include but are not limited to prostate cancer, acne vulgaris, hirsutism, precocious puberty, benign prostatic hyperplasia, seborrhea, androgen alopecia and sexual deviance. Control of androgenic activity may also be useful in male contraception. Estrogen-related diseases include but are not limited to breast cancer, uterine cancer, ovarian cancer, endometriosis, uterine fibroma, precocious puberty and benign prostatic hyperplasia.

The invention further provides a pharmaceutical composition comprising a pharmaceutically acceptable diluent or carrier and a therapeutically effective amount of a sex steroid activity inhibitor having an estrogenic nucleus of formula I: ##STR4## substituted at a ring carbon with at least one side chain represented by the formula --R¹ --B--R² --!_(x) L--G wherein the constituents of said side chain, the location (and preferred locations) for said chain, and the preferred structures and substituents of said nucleus are as defined in the above methods for inhibiting sex steroid activity.

The invention further provides a sex steroid activity inhibiting compound having an estrogenic nucleus of formula I: ##STR5## substituted at a ring carbon with at least one side chain represented by the formula --R¹ --B--R² --!_(x) L--G wherein the constituents and locations (and preferred locations) of said chain, and the preferred structure and substituents of said nucleus are as defined above for the methods of inhibiting sex steroid activity.

The invention further provides an inhibitor of sex steroid activity having, as part of its molecular structure, a substituted or unsubstituted non-steroidal estrogenic nucleus of general formula II: ##STR6## wherein R⁵ and R⁶ are hydrogen lower alkyl, alkoxy carbonyl, (C₁ -C₂₀) alkanoyl, (C₃ -C₂₀) alkenoyl, (C₃ -C₂₀) alkynoyl, (C₇ -C₁₁) aroyl and alkylsilyl,

wherein dotted lines are optional pi bonds. In some embodiments, the optional pi bonds are not simultaneously present when aromaticity would result from such simultaneous presence, wherein R¹⁵ is either a direct bond from e to the number 5 carbon or a methylene or ethylene linkage to the number 5 carbon or a lower alkyl substituent, wherein e is selected from the group consisting of carbon, sulfur and nitrogen, q is absent or is a divalent methyl or ethyl moiety; said inhibitor further having a side chain of the formula --R¹ --B--R² --!_(x) L--G wherein in at least one of said side chains is substituted at position selected from the group consisting of carbon 2, carbon 4, carbon 5, carbon 10, carbon 11, carbon 13, q and on e atom wherein:

x is an integer from 0 to 6, wherein at least one of L and G is a polar moiety distanced from said ring carbon by at least three intervening atoms, and wherein:

R¹ and R² are independently either absent or selected from the group consisting of straight- or branched-chain alkylene, straight- or branch-carbon 2, carbon 4, carbon 5, carbon 10, carbon 11, carbon 13, q and on e atom wherein:

x is an integer from 0 to 6, wherein at least one of L and G is a polar moiety distanced from said ring carbon by at least three intervening atoms, and wherein:

R¹ and R² are independently either absent or selected from the group consisting of straight- or branched-chain alkylene, straight- or branched-chain alkynylene, straight- or branched-chain alkenylene, phenylene, and fluoro-substituted analogs of the foregoing;

B is either absent or selected from the group consisting of --O--, --S--, --Se--, --SO--, --SO₂ --, --NR³ --, --SiR³ ₂ --, --CR³ OR³ --, --NR³ CO--, --NR³ CS--, --CONR³, --CSNR³ --, --COO--, --COS--, --SCO--, --CSS--, --SCS--, --OCO-- and phenylene (R³ being hydrogen or lower alkyl);

L is either a moiety which together with G, forms a heterocyclic ring having at least one nitrogen atom or is selected from the group consisting of lower alkyl, --CONR⁴ --, --CSNR⁴ --, --NR⁵ CO--, --NR⁵ CS--, --NR⁵ CONR⁴ -- ##STR7## --SO₂ NR⁴ --, --CSS--, --SCS--, --(NO)R⁴ --, --(PO)R⁴ --, --NR⁵ COO--, --NR⁵ SO² --, --O--, --NR⁴ --, --S--, --SO-- and --SO₂ -- (R⁴ and R⁵ being independently selected from the group consisting of hydrogen and lower alkyl; and R⁶ being selected from the group consisting of hydrogen, nitrile and nitro); and

G is either a moiety which together with L forms a heterocyclic ring having at least one nitrogen atom or is selected from the group consisting of hydrogen, lower alkyl, lower alkenyl, lower alkynyl, (C₃ -C₇) cycloalkyl, bromo(lower)alkyl, chloro(lower)alkyl, fluoro(lower)alkyl, iodo(lower)alkyl, cyano(lower)alkyl, carboxy(lower)alkyl, (lower)alkoxycarbonyl(lower)alkyl, (C₆ -C₁₀) aryl, (C₇ -C₁₁) arylalkyl, di(lower)alkylamino(lower)alkyl, fluoro-substituted analogs of the foregoing.

This invention further provides a pharmaceutical composition comprising a pharmaceutically acceptable diluent or carrier and a therapeutically effective amount of a sex steroid activity inhibitor having, as part of its molecular structure, a substituted or insubstituted estrogenic nucleus of general structure II, ##STR8## wherein dotted lines are optional pi bonds; wherein e is selected from the group consisting of carbon, sulfur and nitrogen, q is absent or selected from the group consisting of a divalent methyl moiety and a divalent ethyl moiety; R¹⁵ is selected from the group consisting of a lower alkyl substitutent, a direct bond from e to the number 5 carbon, a methyle linkage from e to the number 5 carbon; said sex steroid inhibitor further including, as another part of its molecular structure, a side chain substitution onto at least one positive said general structure II wherein said side chain has the general formula --R¹ --B--R² --!L--G as defined above.

The inhibitor is preferably hydroxy substituted in at least the 3 or 12 positions, and is preferably substituted at the 7 position with a C₁ -C₄ alkyl. Compounds of formula II above may be used, preferably of pharmaceutical compositions including acceptable diluents or carriers, to treat sex steroid dependent diseases by inhibiting sex steroid activity.

As used herein, the term "sex steroid activity inhibitor" includes any compound which suppresses the activity of sex steroids by any mechanism including, for example, inhibition of sex steroid synthesis or antagonistic blocking of sex steroid receptors. "Androgen activity inhibitors" and "estrogen activity inhibitors" are sex steroid inhibitors capable of inhibiting the activity of androgens and estrogens, respectively. For example, estrogen activity inhibitors include, but are not limited to antiestrogens which block estrogen receptors, thereby making them unavailable to estrogen compounds which could otherwise activate those receptors. Sex steroid activity inhibitors also include compounds which inhibit the formation of compounds capable of activating sex steroid receptors such as inhibitors of the production of natural sex steroids (e.g. 17β-estradiol) or inhibitors of production of precursors of natural sex steroids. One mechanism by which these sex steroid production inhibitors may operate is by blocking enzymes which catalyze production of natural sex steroids or their precursors (e.g. enzymes such as aromatase, 17β-hydroxysteroid dehydrogenase, 3β-hydroxysteroid dehydrogenase and the like).

As used herein, the term "estrogenic nucleus" includes any compound which, in the absence of the side chain substituent specified herein, is capable of acting as an estrogen as determined by a weight increase of least 100 percent over a seven-day period of the uterus of ovariectomized rats treated with the compound in question (0.5 mg twice daily per grams of body weight) versus a control group of ovariectomized rats. Treatment should start on the day of castration. The precise test, other than any parameters set forth in this paragraph, is that reported in Simard et al., Mol. Endocrinol. 2:775-784 (1988).

The following conventions apply to structural formulae see forth herein. Unless specifically designated to the contrary, substituents may have either α or β stereochemistry or, where valence permits may represent one substituent in α position and another in β position. Presence of optional pi bonds are independent of each other. All structures include salts thereof. Atoms of any estrogenic nucleus for which no substituent is shown or described may optionally be substituted or unsubstituted so long as such substitution does not prevent the nucleus from functioning as an "estrogenic nucleus" as defined herein. Those atoms having a defined substituent may optionally be further substituted by other substituents where their valence permits such further substitution. As used herein the term "lower" when describing a chemical moiety means a moiety having 8 or fewer atoms. For instance, a "lower alkyl" means a C₁ to C₈ alkyl. Any moiety of more than two atoms may be straight- or branched-chain unless otherwise specified.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a graph illustrating the antiestrogenic activity of one preferred antiestrogen of the invention as compared to a prior art steroidal antiestrogen N-n-butyl-N-methyl-11-(3', 17'B-dihydroxyestra-1',3', 5'(10')trien-7'a-yl)undecenamide as described in E.P. Patent 138504.

FIG. 2 is a graph illustrating that the antiestrogen which is the subject of FIG. 1 is also a good inhibitor of sex steroid synthesis.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

Preferred methods of treating of sex steroid-related diseases, especially estrogen-related diseases, and preferred methods of blocking estrogen receptors comprise administering to a patient in need of such treatment, a therapeutically effective amount of a sex steroid-activity inhibitors as defined above.

Preferred estrogenic nuclei suitable for use in accordance with the invention include but are not limited to estradiol and derivatives thereof. Other suitable estrogenic nuclei include but are not limited to those which (as reported in the references set forth below) effect more than the threshold increase in uterine weight of ovariectomized rats set forth above as defining an estrogenic nucleus (Simard et al., Mol. Endocrinol. 2:775-784 (1988).

Some preferred estrogenic nuclei include but are not limited to: ##STR9## wherein x is a halogen, preferably chlorine or bromine; wherein R₃ and R₄ are independently selected from the group consisting of hydrogen, lower alkyl, lower alkoxy carbonyl, (C₁ -C₂₀), alkanoyl, (C₃ -C₂₀) alkenoyl, (C₃ -C₂₀) alkynoyl and (C₇ -C₁₁) aroyl, alkylsilyl, 1-alkyloxy-alkyl and 1-alkyloxy cycloalkyl. ##STR10## wherein R₃ is selected from the group consisting of hydrogen, lower alkyl, lower alkoxy carbonyl, (C₁ -C₂₀), alkanoyl, (C₃ -C₂₀) alkenoyl, (C₃ -C₂₀) alkynoyl and (C₇ -C₁₁) aroyl, alkylsilyl, 1-alkyloxy-alkyl and 1-alkyloxy cycloalkyl. ##STR11## wherein R₃ is selected from the group consisting of hydrogen, lower alkyl, lower alkoxy carbonyl, (C₁ -C₂₀), alkanoyl, (C₃ -C₂₀) alkenoyl, (C₃ -C₂₀) alkynoyl and (C₇ -C₁₁) aroyl, alkylsilyl, 1-alkyloxy-alkyl and 1-alkyloxy cycloalkyl. ##STR12## wherein R₃ is selected from the group consisting of hydrogen, lower alkyl, lower alkoxy carbonyl, (C₁ -C₂₀), alkanoyl, (C₃ -C₂₀) alkenoyl, (C₃ -C₂₀) alkynoyl and (C₇ -C₁₁) aroyl, alkylsilyl, 1-alkyloxy-alkyl and 1-alkyloxy cycloalkyl. ##STR13## wherein R₃ is selected from the group consisting of hydrogens, lower alkyl, lower alkoxy carbonyl, (C₁ -C₂₀), alkanoyl, (C₃ -C₂₀) alkenoyl, (C₃ -C₂₀) alkynoyl and (C₇ -C₁₁) aroyl, alkylsilyl, 1-alkyloxy-alkyl and 1-alkyloxy cycloalkyl. ##STR14## wherein the dotted lines are optional double bonds; wherein R₅ and R₆ are independently selected from the group consisting of hydrogen, lower alkyl, lower alkoxy carbonyl, (C₁ -C₂₀), alkanoyl, (C₃ -C₂₀) alkenoyl, (C₃ -C₂₀) alkynoyl and C₇ -C₁₁) aroyl, alkylsilyl, 1-alkyloxy-alkyl and 1-alkyloxy cycloalkyl. ##STR15## wherein the dotted lines are optional double bonds; wherein R₅ and R₆ are independently selected from the group consisting of hydrogens, lower alkyl, lower alkoxy carbonyl, (C₁ -C₂₀), alkanoyl, (C₃ -C₂₀) alkenoyl, (C₃ -C₂₀) alkynoyl and (C₇ -C₁₁) aroyl, alkylsilyl, 1-alkyloxy-alkyl and 1-alkyloxy cycloalkyl. ##STR16## wherein q is absent, methylene or ethylene wherein R₅ and R₆ are independently selected from the group consisting of hydrogens, lower alkyl, lower alkoxy carbonyl, (C₁ -C₂₀), alkanoyl, (C₃ -C₂₀) alkenoyl, (C₃ -C₂₀) alkynoyl and C₇ -C₁₁) aroyl, alkylsilyl, 1-alkyloxy-alkyl and 1-alkyloxy cycloalkyl.

Preferred sex steroid activity inhibitors result from substituting estrogenic nucleic with the preferred substituents set forth herein, including the side chain --R¹ -- B--R² !L--G as defined above. Preferred sex steroid activity inhibitors in accordance with the invention include but are not limited to: ##STR17## When sex steroid activity inhibitors are administered in accordance with the invention, they are preferably administered as a dosage from about 1 mg to about 2000 mg of active expedient (i.e. sex steroid activity inhibitor), per day per 50 kg of body weight, most preferably from about 10 mg to about 100 mg per day per kg of body weight.

The sex steroid activity inhibitors are preferably prepared as pharmaceutical compositions together with pharmaceutically acceptable carriers and diluents. When prepared for parenteral injection, an inhibitor of sex steroid activity is preferably added at a concentration between about 1 mg/ml and about 100 mg/ml (preferably about 2 mg/ml to about 10 mg/ml) into a carrier preferably selected from the group consisting of saline, water, aqueous ethanol, aqueous dimethylsulfoxide and oil.

When a pharmaceutical composition of the invention is prepared for oral ingestion, the composition preferably includes at least one inhibitor of sex steroid activity wherein the total concentration of all such inhibitors in said pharmaceutical composition is from about 1% to about 95% of the composition (by weight), and preferably from about 5% to about 20%. The composition preferably further includes a pharmaceutically acceptable diluent, for example, starch or lactose with or without tartrazine. Slow release pharmaceutical products comprising the novel inhibitors of sex steroid activity may be incorporated into slow release pharmaceutical products which, other than addition of the novel inhibitors, may be prepared by known methods and administered orally as well as parenterally.

In the side-chain structure, L is preferably separated from the androgenic nucleus by at least 3 intervening and preferably 6 atoms. A polar moiety (G, L or both) is preferably separated from the androgenic nucleus by at least 8 intervening atoms. It is also preferred that the side chain R¹ --B--R² --!_(x) L--G have between about 7 and 30 carbon atoms.

EXAMPLES OF SYNTHESIS OR PREFERRED INHIBITORS OF SEX STEROID ACTIVITY

INSTRUMENTATION

The IR spectra were taken on a Perkin-Elmer 1310 spectrophotometer. Proton NMR spectra were recorded on a Varian EM-360A (60 MHz, when specified) or a Varian XL-200 (MHz) instrument. The following abbreviations have been used: s, singlet; d, doublet; dd, doublet of doublet; t, triplet; q, quadruplet; and m, multipier. Chemical shifts are reported in δ values in ppm relative to tetramethysilane (TMS) as internal standard. Mass spectra (MS) were obtained on a V.G. Micromss 16F machine. Thin-layer chromatography (TLC) was performed on 0.25 mm KieselSel 60F254 plates (E. Merck, Darmstadt, FRG). For flash chromatography, Merck-Kieselgel 60(230-400 mesh A.S.T.M.) was used. All solvents used in chromatography has been distilled. Unless otherwise note, starting material and reactant were obtained commercially and were used as such or purified by standard means. All solvents and reactants purified and dried were stored under argon. Anhydrous reactions were performed under an inert atmosphere, the set-up assembled and cooled under argon. Organic solutions were dried over magnesium sulfate, evaporated on a rotatory evaporator and under reduced pressure. Anhydrous solvents were prepared in the following way.

    ______________________________________                                         SOLVENT             DISTILLED OVER                                             ______________________________________                                         AMINE, DIMETHYLFORMAMIDE                                                                           CaH.sub.2                                                  HEXANE, DICHLOROMETHANE                                                                            P.sub.2 O.sub.5                                            ACETONE             K.sub.2 CO.sub.3                                           BENZENE             LiAlH.sub.4                                                TOLUENE             Na                                                         ETHER, TETRAHYDROFURAN                                                                             LiAlH.sub.4, Na Benzophenone                               ______________________________________                                    

EXAMPLE-1 Synthesis of Preferred Sex Steroid Activity Inhibitors

Synthesis of a starting compound, N-n-butyl, N-methyl-11-(3'-benzoyloxy-17'-oxo-estra-1',3',5'(10')-trien-7'α-yl)undecanamide (9) (SCHEME 1)

19-nor-testosterone acetate 3-enolacetate (2)

In an apparatus supplied with a drierite drying tube, a solution of 19-nor-testosterone (1) (100 g; 0.365 mole) in acetic anhydride (200 ml), pyridine (32 ml) and acetylchloride (320 ml) was heated at reflux under magnetic stirring, for 3 h and then concentrated to dryness under vacuum. The dry residue was triturated in absolute ethanol, filtered and washed with little portions of absolute ethanol. After drying, 19-nor-testosterone acetate 3-enolacetate was obtained as a white powder (121.4 g, yield 93%) mp. 176°-177° C. The structure was confirmed by spectroscopic means.

17β-acetoxy-estra-4,6-dien-3-one (3)

To a cooled suspension of enolacetate (121 g; 0.337 mole) in a mixture of DMF (330 ml) and water (7.2 ml) at 0° C. was added, under nitrogen, over a period of 1 h, N-bromosuccinimide (63 g). The resulting solution was stirred for an additional 0.5 h at 0° C. Then lithium carbonate (60.8 g) and lithium bromide (30.4 g) were added. The mixture was heated at 95° C. for 3 h and then poured into 1.7 l of ice-cold water containing 165 ml of glacial acetic acid. After stirring during 15 hours, the crude 17β-acetoxy-estra-4,6-dien3-one (3) was filtered, washed with water, dried in a desiccating apparatus and recrystallized twice from isopropyl ether (72 g, yield 68%, mp 110° C.). The structure was confirmed by spectroscopic means.

7α-(11'-acetoxy-undecyl)17β-acetoxy estra-4-en-3-one (4)

A. Preparation of reagents and solvents

11-bromo undecanol tetrahydro pyranyl ether

11-bromo-undecanol (100 g, 398 mmol) was dissolved in dry ether (768 ml) and the solution was cooled to 0° C. using an ice/H₂ O bath. To this solution was added HCl gas (2.13 g, 58.4 mmol, 26 ml of HCl/ether).

To this mixture, a solution of 3,4-dihydro-2H-pyran (39.9 g, 43.3 ml) freshly distilled in dry ether (218 ml) was added over a period of 90 min. The solution was then stirred over a period of 16 hours at room temperature. Afterwards, sodium bicarbonate was added to the mixture. The residue was filtered and the solvent was evaporated under vacuum.

The product was then filtered through basic alumina (250 g, Woelm, grade II) using petroleum ether (30-60) as solvent (112 g, 81%).

B. Grignard reagent

In a dry three-neck flask (1000 ml) under dry argon, magnesium (12.0 g, 494 mmol) was placed and activated with iodine. Magnesium was heated with the flame to remove iodine and to dry the apparatus. The system was then cooled to -20° C., and a solution of 11-bromo-undecanol tetrahydro pyranyl ether (73.8 g, 211 mmol) in dry THF (420 ml) was added dropwise. The mixture was stirred under dry argon during one day at -20° C.

The mixture was cooled to -35° C. (±2° C.) using a dry ice/CCL₄ /acetone bath. The anhydrous cuprous chloride (1.18 g, 12 mmol) was added and the mixture was stirred over a period of 0.5 h.

C. Addition of Grignard reagent

After 0.5 h, using the same apparatus mentioned above (Ar, -35° C.), a solution of 17β-acetoxy estra-4,6-diene-3-one (3) (32.0 g, 102 mmol) in dry THF (300 ml) was added dropwise over a period of 6 h to the Grignard reagent (red coloration appeared and disappeared). The mixture was stirred for an additional 1 h and, after removal the cooling bath, acidified (about 0° C.) with acetic acid (40 ml), diluted with water and extracted with ether (3×). The ether solution was washed with a saturated sodium bicarbonate solution and water. The organic layer was dried over anhydrous magnesium sulfate and evaporated under reduced pressure to dryness.

The residue was dissolved in HeOH (660 ml) and 5N HCl (180 ml), refluxed for 1 h and 45 min, then concentrated under reduced pressure and cooled in an ice bath. The mixture was then filtered to remove the white precipitate. After the solution had been diluted with water and extracted with methylene chloride (3×), the organic layer was dried over anhydrous MgSO₄ and evaporated under reduced pressure to dryness. Finally, the product (55.9 g, brown oil) was chromatographed on silica gel (Kieselgel 60F254, Merck, 0.063-0.200 mm, 1500 g). Elution with mixtures of methylene chloride and ethyl acetate (4:1 to 1:2 v/v) and then pure ethyl acetate gave crude 7α-(11'-hydroxy-undecyl)-17β-hydroxy estra-4-en-3-one (34.8 g) which was dissolved in dry pyridine (200 ml) and dry acetic anhydride (200 ml), stirred 17 h at room temperature and then poured in ice-water. The product was extracted with methylene chloride (3×), washed with 1N hydrochloric acid, water, saturated sodium bicarbonate and water (3×), dried on anhydrous magnesium sulfate and filtered. After evaporation of solvent, the mixture (35 g) of 7α- and 7β-diacetoxyenones and degradation products of Grignard reagent were separated by flash chromatography on silica gel (Kieselgel 60, Merck, 230 mesh ASTM, 2.0 kg) developed with a mixture of hexane and diethyl ether (2:3 v/v). The first product eluted was pure amorphous 7α-(11'-acetoxyundecyl)17β-acetoxy-estra-4-en-3-one, (4) (20.8 g, 39.4 mmol, yield from dienone was 39.0%). Further elution gave the 7β-isomer (5) (5.4 g, 10.3 mmol, 10%). All structures were determined by spectroscopic means.

7α-(11'-hydroxy-undecyl)estra-1,3,5(10)-trien-3,17β-diol (6a)

Under dry argon, a solution of 7α-(11'-acetoxyundecyl) 17β-acetoxy-estra-4-en-3-one (4) (17.0 g, 32.4 mmol) in dry acetonitrile (150 ml) was added rapidly to a suspension of cupric bromide (14.8 g, 66.2 mmol) and mmol) and lithium bromide (2.89 g, 33.6 mmol) in warm acetonitrile (75 ml). The mixture was heated to reflux over a period of 30 min and stirred vigorously, and then cooled to room temperature. A saturated aqueous solution of sodium bicarbonate (50 ml) was added, and then the organic compound was extracted with ethyl acetate (3×150 ml). The organic layers were washed with water, dried over anhydrous magnesium sulfate, filtered and evaporated under vacuum to dryness. The residue was chromatographed on silica gel (Kieselgel 60F254 Merck 0.063-0.200 mm; 1000 g). Elution with hexane-ethyl acetate (1:1 v/v) gave the 7α-(11'-acetoxy-undecyl)estra-1',3',5'(10')-trien-3,17β-diol, 17β-acetate (6b) (8.51 g; 50.3%) and the starting product (1.33 g; 15%).

The above diacetate phenol (8.51 g, 16.2 mmol) was dissolved in methanol (90 ml) and sodium hydroxide 30% (w/v) (9 ml). The mixture was refluxed for 90 min under dry nitrogen. The solution was then concentrated under vacuum and diluted with hydrochloric acid (10% v/v). The mixture was extracted using ethyl acetate (4×150 ml) and the ethyl acetate extract was washed with water, dried over anhydrous magnesium sulfate, filtered and evaporated under vacuum. The evaporation gave 7α-(11'-hydroxy undecyl)estra-1,3,5(10)-trien-3,17β-diol (6a) (6.99 g, 98% brut) as a yellow foam, the structure of which was confirmed by spectroscopic means.

3-benzoyloxy 7α-(11'-hydroxy undecyl)estra-1,3,5(10)-trien-17β-ol (7)

The above triol (6.99 g; 15.8 mmol) was dissolved in acetone (25 ml) and an aqueous solution of sodium hydroxide (1N, 19.1 ml). The mixture was cooled to 0° C. using an ice/water bath. Benzoyl chloride (2.22 ml, 19.1 mmol) was then added dropwise. The mixture was stirred for 40 min at 0° C. and then diluted with water. The solution was extracted using ethyl acetate (3×) and the organic layers were washed with a saturated aqueous solution of sodium bicarbonate and finally with water. The ethyl acetate solution was dried over anhydrous magnesium sulfate, filtered and evaporated under vacuum to dryness. Then, the residue was immediately chromatographed on silica gel (Kieselgel, 60F254, 0.063-0.200 mm; 500 g). The chromatography was carried out, first, using methylene chloride as solvent (about 1 liter) and secondly the pure 3-benzoyloxy 7α-(11'-hydroxy undecyl)estra-1,3,5(10)-trien-17β-ol (7), colorless oil (6.50 g, 75%) was eluted with methylene chloride-ethyl acetate (5:1 about 1 liter and 4:1; v/v). The structure was confirmed by spectroscopic means.

11-(3'-benzoyloxy-17'-oxo-estra-1',3',5'(10')-trien-7α-yl)undecanoic acid (8)

To a cooled solution of 3-benzoyloxy-7α-(11'-hydroxy undecyl)estra-1,3,5(10)-trien-17β-ol (7) (4.3 g) in acetone (100 ml) was added dropwise Jone's reagent (8N-chromic acid solution, 6.7 ml). After 30 min, isopropanol (40 ml) was added and the mixture was concentrated under vacuo. Water was added and the mixture was extracted four times with ethyl acetate. The organic layers were washed twice with brine, dried over magnesium sulfate and evaporated to dryness. The crude 11-(3'-benzoyloxy-17'-oxo-estra-1',3',5'(10')-trien-7'α-yl)undecanoic acid (8) (3.94 g) was used in the next step without purification. ##STR18## N-n-butyl,n-methyl-11-(3'-hydroxy-17'-oxo-estra-1',3',5'(10')-trien-7'.alpha.-yl)undacanamide (9b)

To 11-(3'-benzoyloxy-17'-oxo-estra-1',3',5'(10')-trien-7'α-yl)undecanoic acid (8) (3.94 g, 7.22 mmol), dissolved in anhydrous CH₂ Cl₂ (100 ml) and cooled at -10° C. was added tributylamine (2.18 ml, 9.15 mmol) and isobutylchloroformate (1.30 ml, 10.0 mmol). The solution was stirred during 35 min. and N-methylbutylamine (13 ml, 109.7 mmol) was added. The mixture was warmed to room temperature and stirred during 1 h. Afterward, CH₂ Cl₂ was added and the organic phase was washed with 1N HCl, water, saturated sodium bicarbonate solution and finally with water, dried with anhydrous MgSO₄ and the solvent was removed under reduced pressure. The residue was purified by chromatography on silica gel. Elution with mixture of EtOAc/hexane (1.5:8.5 v/v) yielded N-butyl, N-methyl-11-(3'-benzoyloxy-17'-oxo-estra-1',3',5'(10')-trien-7'α-yl)undecanamide (9a) (4.25 g, 96%) as colorless oil; IR ν (neat) 1750, 1725 and 1640 cm⁻¹. The above described benzoyloxy amide (341 mg, 0.54 mmol) was dissolved in methanol (10 ml) and cooled at 0° C. Following this 2N NaOH (5 ml) was added and the mixture was stirred during 60 min. at 0° C. The solution was neutralized with 1N HCl and extracted with CH₂ Cl₂. The organic phase was dried with anhydrous MgSO₄ and the solvent was removed under reduced pressure. The residue was purified by chromatography on silica gel. Elution with mixture of EtOAc/hexane (3:7 v/v) yielded N-butyl, N-methyl-11-(3'- hydroxy-17'-oxo-estra-1',3',4'(10)-trien-7'α-yl)undecanamide (9b) (284 mg, 97%) as colorless oil; ¹ H-NMR δ(CDCl₃) 0.91 (s,3H,18'-CH₃), 2.76 app(d,1HJ=16,3 Hz, part of ABX system, 6'-H) 2.96 and 2.98 (2s,3H N--CH₃) 3.27 and 3.38 (2t_(app),2H,J=7.5 Hz,N--CH₂ --) 6.63 (broad s,1H,4'-H), 6.70 (broad d,1H,J=8.5 Hz,2'-H), 7.12 (d,1H,J=8.4 Hz,1'-H); IR ν_(max) (neat) 3270, 1730, 1615 cm⁻¹ ; MS m/e 523 (M⁺, 100%), 508 (M⁺ -CH₃, 32%), 142 (C₂ H₄ CON(CH₃)C₄ H₉ ⁺, 47%).

16-Halo-estradiol undecanamide (Scheme 2)

N-n-butyl, N-methyl-11-(3',17'-diacetoxy-estra-1',3',5'(10'),16'-tetraen-7'α-yl)undecanamide (10)

The ketone amide 9b (163 mg, 0.50mmol) was dissolved in isoprenyl acetate (10 ml). p-toluenesulfonic acid (44 mg) was then added and the solution was distilled to about two-thirds of the original volume in 7 h and was then stirred at reflux for 12 h. Afterwards, the solution was cooled with an ice-water bath and extracted with 50 ml of cooled ether. The ether was washed with a cooled saturated sodium bicarbonate and water. The organic phase was dried with anhydrous MgSO₄ and the solvent was removed under reduced pressure. The residue was filtered through alumina (15 mm×50 mm alumina Woehlm neutral, activity II) using a mixture of benzene-diethyl ether (3:7 v/v) as eluant. The solvent was removed under reduced pressure and, the residue was purified by flash chromatography on silica gel. Elution with mixture of EtOAc/hexane (1:4 v/v) yielded the N-butyl, N-methyl-11-(3',17'-diacetoxy-estra-1',3',5'(10'), 16'-tetraen-7'α-yl)undecanamide (10) (244 mg, 80%) as colorless oil; ¹ H-NMR β_(m) (CDCl₃) 0.92 (s,3H,18'-CH₃), 0.92 and 0.95 (2t,3H,J=7.0 Hz,N(CH₂)₃ CH₃), 2.18 (s,3H,17'-OCOCH₃), 2.28(s,3H,3'-OCOCH₃), 2.76 app (d,1H,J=16.1Hz, part of ABX system,6'-H), 2.90 and 2.96 (2s,3H,N--CH₃), 3.26 and 3.35 (2t_(app),2H J=7.6 Hz,N--CH₂ --) 5.52 (m,1H,16'-H) 6.80 (broad s,1H,4'-H), 6.85 (dd,1H,J₁ =9.1 Hz and J₂ =3.0 Hz,2'-H), 7.27 (d,1H,J=9.1 Hz,1'-H); IR ν_(max) (neat) 1750, 1635, 1200 cm⁻¹ ; MS m/e 607 (M⁺,2%), 5(M⁺ -COCH₂, 100%), 550 (M⁺ -COCH₂ --CH₃,13%), 523 (M⁺ --2COCH₂,45%), 142 (C₂ H₄ CON(CH₃)C₄ H₉ ⁺, 55% 129 (C₄ H₉ (CH₃)NCOCH₃ ⁺,38%), 114 (C₄ H₉ (CH₃)NCO⁺, 60%), 86 (C₄ H₉ (CH₃)N⁺, 25%); EXACT MASS calcd for C₃₈ H₅₇ O₅ N 607.4239, found 607.4234.

N-butyl, N-methyl-11-(16'α-chloro-3'acetoxy-17'-oxo-estra-1',3',4'(10')-triene-7'α-yl)undecanamide (11, X═Cl)

To diacetate amide 10, dissolved in 5 ml of acetone, was added a solution of sodium acetate (2.6 equivalents) in acetic acid and water (1:11.3 v/v) and then, was treated with tertbutyl hypochlorite (1 eq.) prepared from t-butanol (4 ml) and Javel water (Javex 6.1%, 50 ml). The clear solution was warmed to 55° C. and stirred for 1 h. Afterwards, the solvent was evaporated to dryness. The residue was dissolved in ether (100 ml) and water was added (20 ml). The organic phase was washed with water, dried with anhydrous MgSO₄ and evaporated to dryness. The residue was purified by chromatography on silica gel carried out with mixture of EtOAc/hexane (3:7 v/v) to give the N-butyl, N-methyl-11-(16'α-chloro-3'-acetoxy-17'-oxo-estra-1',3',4'(10')-trien-7'α-yl)undecanamide 11, X═Cl) (115 mg, 89%) as colorless oil; ¹ H-NMR ν (CDCl₃) 0.92 and 0.95 (2t,3H,J=7.0 Hz,N(CH₂)₃ CH₃), 0.96 (s,3H,18'-CH₃), 2.28 (s,3H,3'-OCOCH₃), 2.80 app (d,1H,J=16,6 Hz, part of ABX system, 6'-H) 2.90 and 2.96 (2s,3H,N--CH₃), 3.24 and 3.35 (2t_(app),2H,J=7.4 Hz,--N--CH₂ --), 4.46 (d,1H,J=6.6 Hz,16'β-H), 6.82 (broad s,1H,4'-H), 6.86 (dd,1H,J=9.1 Hz and J₂ =,2.6 Hz,2'-H), 7.29 (d,1H,J=9.1 Hz,1'-H); IR ν_(max) (neat) 1750, 1640, 1205 cm⁻¹ ; MS m/e 601, 599 (M⁺,24%, 68%), 142 (C₂ H₄ CON(CH₃)C₄ H₉ ⁺, 100%), 114 (C₄ H₉ (CH₃)NCO⁺,93%).

N-butyl, N-methyl-11-(16α-chloro-3',17'-dihydroxy-estra-1',3',5'(10')-trien-7'α-yl)undecanamide ("EM 139") and ("EM 170")

A stirred solution of haloketone amide (11, X═Cl) in anhydrous tetrahydrofuran (THF) (10 ml) under arson was chilled to -70° C. with 2-propanol/dry ice bath. A solution of 1.0M of lithium aluminium hybride (2 eq.) was then added dropwise. After 30 min, the reaction was allowed to return slowly at 0° C. for 5 min, then was quenched by the dropwise addition of a mixture of THF-EtOAc (5 ml) (1:1 v/v) and acidified at pH˜4 with (10%) HCl. The mixture was stirring for 5 min at room temperature and then extracted with EtOAc. The organic phase was washed with water, dried on anhydrous Na₂ SO₄ and evaporated under reduced pressure. The residue was chromatographed on silica gel with a mixture of EtoOAc/hexane (4:6 v/v) as eluant:

N-butyl, N-methyl-11-(16'α-chloro-3'17'α-dihydroxy-estra-1',3',5'(10')-trien-7'α-yl)undecanamide ("EM 170")

(15 mg, 29%) as colorless oil; analytical sample was obtained by HPLC purification; ¹ H-NMR δ(CDCl₃, 400 MHz) 0.79 (s,3H,18'-CH₃), 0.93 and 0.96 (2t, 3H,J=7.3 Hz,N(CH₂)₃ CH₃), 2.80 (2H,J₆,6 =17.1 Hz and J₆,7 =4.5 Hz, Δδ=24.34 (Hz, system ABX, 6'-H), 2.94 and 2.99 (2s, 3H,N--CH₃), 3.26 (dd,J₁ =7.6 Hz and J₂ =7.4 Hz) and 3.32-3.43 (m)- 2H,--N--CH₂ --!, 3.71 (d,1H,J=4.5 Hz,17'β-H), 4.63 (ddd, 1H, J₁₆,15 =10.2 Hz, J₁₅,17 -=4.5 Hz and J₁₆,15 3.9 Hz, 16'β-H), 6.50 (d, 1H, J=24 Hz, 3'-OH), 6.60 (d, 1H,J=2.5 Hz, 4'-H), 6.66 (dd,1H,J₁ =8.4 Hz and J₂ =2.5 Hz, 2'-H), 7.14 (d,1H J=8.5 Hz, 1'-H); IR ν_(max) (neat) 3300, 1615 1495 cm⁻¹ ; MS m/e 561,559 (M⁺, 40%, 100%), 523 (M⁺ -HCl, 20%), 142 (C₂ H₄ CON(CH₃)C₄ H₉ ⁺, 44%), 114 (C₄ H₉ (CH₃)CNO⁺, 37%); Exact mass calculated for C₃₄ H₅₄ O₃ N³⁵ Cl 559.3785, found 559.3821; and

--N-butyl, N-methyl-11-(16'α-chloro-3',17'β-dihydroxy-estra-1'3',5'(10')-trien-7'α-yl)undecanamide ("EM 139")

(25 mg, 55%) as a colorless oil; analytical sample was obtained by HPLC purification; 1H-NMR δ(CDCl₃, 400 MHz), 0.81 (s,3H, 18'-CH₃), 0.93 and 0.96 (2t, 3H,J=7.3 Hz, (CH₂)₃ CH₃), 2.78 (2H, J₆,6 =16.2 Hz and J₆,7 =4.5 Hz, Δ⁵ =24.34 Hz, system ABX, 6'-H), 2.94 and 2.99 (2s, 3H,N--CH₃), 3.27 (dd, J₁ =7.6 Hz and J₂ =7.5 Hz) and 3.31-3.45 (M) 2H, --N--CH₂ --!, 3.86 (dd, 1H, J₁₇,17 -_(OH) =3.4 Hz and J₁₇,16 =5.9 Hz, 17'α-H), 4.11 (ddd, 1H, J₁₆,15 =10.8 Hz, J₁₆,17 =5.9 Hz and 4.11 (ddd, 1H, J₁₆,15 =10.8 Hz, J₁₆,17 =5.9 Hz and J₁₆,15 =2.5 Hz, 16'β-H), 6.56 (d, 1H, J=19.7 Hz, 3'-OH), 6.61 (d, 1H, J=2.5 Hz, 4'-H), 6.66 (dd, 1H, J₁ =8.4 Hz and J₂ =2.6 Hz, 2'-H), 7.13 (d, 1H, J=8.4 Hz, 1'-H); IR ν_(max) (neat) 3320, 1615, 1490 cm⁻¹ : MS m/e 561,559 (M⁺, 38%, 100%), 523 (M⁺ -HCl, 16%), 142 (C₂ H₄ CON(CH₃)C₄ H₉ ⁺, 80%), 114 (C₄ H₉ (CH₃)NCO⁺,76%); exact mass calculated for C₃₄ H₅₄ O₃ N³⁵ Cl 559.3785, found 559.3825. ##STR19## N-n-butyl, N-methyl-11-(16'α-bromo-3'-acetoxy-17'-oxo-estra-1',3',5'(10'),trien-7'α-yl)undecanamide (11, X═Br)

To the above diacetate 10 (244 mg, 0.40 mmol) dissolved in 10 ml of acetic acid was added dropwise with stirring within 10 minutes and at room temperature, a brominating solution composed of 50 mg (0.6 mmol) of sodium acetate, 1.6 ml of acetic acid, 0.04 ml of water and 63.9 mg (0.02 ml, 0.40 mmol) of bromine. During the course of this reaction, a red coloration appeared and disappeared. To the solution, 50 ml of ether was added and the organic phase was washed with water (4×50 ml) followed by a saturated sodium bicarbonate solution (2×50 ml) and finally with water (3×50 ml). The combined phase was dried over anhydrous magnesium sulfate and the solvent was removed in vacuo. The residue was chromatographed on silica gel (Kieselgel, 60F254, Merck, 0.063-0.200 mm). Elution with a mixture of hexane-ethyl acetate (4:1 v/v) yielded N-butyl, N-methyl-11-(16α-bromo-3'-acetoxy-17'-oxo-estra-1',3',5'(10'),trien-7'-α-yl)undecanamide (11, X═Br) (201 mg, 78%) as colorless oil (201 mg, 78%), as colorless oil; ¹ H-NMR o (CDCl₃), 0.94 (s, 3H,18'-CH₃), 2.28 (s, 3H, 3'-OCOCH₃), 2.82 app (d,1H,J=16.4 Hz, part of ABX system, 6'-H), 2.90 and 2.96 (2s, 3H,N--CH₃), 3.24 and 3.35 (2t_(app), 2H, J=7.7 Hz, --N--CH₂ --), 4.58 (t,1H,J=3.6 Hz, 16β-H), 6.82 (broad s,1H,4'-H), 6.88 (dd,1H, J=8.0 Hz and J₂ =4.0 Hz,2'-H), 7.29 (d,1H, J=8.0 Hz, 1'-H,); MS m/e 644 (M⁺,7%), 565 (M⁺ -Br, 77%), 522 (M⁺ -Br--COCH₂, 55%), 142 (C₂ H₄ CON(CH₃)C₄ H₉ ⁺, 67%), 114 (C₄ H₉ (CH₃)NCO⁺, 66%), 88 (100%).

N-butyl, N-methyl-11-(16'α-bromo-3',17'-dihydroxy-estra-1',3,4'(10')-trien-7'α-yl)undecanamide ("EM 105") and ("EM 171")

A solution of bromoketone amide 11 (X═Br) (295 mg, 0.46 mmol) in anhydrous tetrahydrofuran (10 ml) under argon was chilled to -70° C. and a solution of 1.0M of lithium aluminium hybride in ether (0.92 ml, 0.92 mmol) was added dropwise with rapid magnetic stirring. After 30 min, the reaction was quenched by the dropwise addition of a mixture of THF-ethyl acetate (1:1 v/v) and acidified by 10% hydrochloric acid. The mixture was stirring for 5 min at room temperature and then extracted with ethyl acetate. The organic phase was washed with water, dried on anhydrous sodium sulfate and evaporated to dryness under reduced pressure. The residue was purified by chromatography on silica gel. Elution with a mixture of hexane-ethyl acetate (7:3 v/v) gave:

N-n-butyl, N-methyl-11-(16'α-bromo-3',17'α-dihydroxy-estra-1',3',5'(10')-trien-7'α-yl)undecanamide ("EM 171")

(63 mg, 211) as colorless oil; ¹ H-NMR δ(CDCl₃, 400 MHz) 0.81 (s, 3H, 18'-CH₃), 0.93 and 0.96 (2t, 3H,J=7.3 Hz,N(CH₂)₃ CH₃), 2.79 (2H,J₆,6 =16.6 Hz, J₆,7 =4.7 Hz, =Δδ=24.34 Hz, system ABX,6'-H), 2.94 and 2.99 (2s,3H,N--CH₃), 3.27 (dd,2H,J₁ =7.7 Hz and J₂ =7.5 Hz, --N--CH₂ --), 3.31-3.44 (m,2H,--N--CH₂ --), 3.66 (dd,1H,J₁₇,17 =1.4 Hz, J₁₇,16 =4,3 Hz, 17'α-H), 4.68 (dt,1H,J₁₆,17 =4,3 Hz, m, J₁₆,15 =9.7 Hz,16'β-H), 6.60 (d,1H,J=2.4 Hz, 4'-H), 6.65 (dd, 1H,J=8.5 Hz and J₂ =2.5 Hz, 2'-H), 7.14 (d,1H,J=8.5 Hz, 1'-H); IR ν_(max) (neat) 3300, 1615, 1495 cm⁻¹ ; MS m/e 605,603 (M⁺, 17%), 523 (M⁺ -HBr, 81%), 142 (C₂ H₄ CON(CH₃)C₄ H₉ ⁺,100%), 114 (C₄ H₉ (CH₃)NCO⁺, 97%); Exact mass calculated for C₃₄ H₅₄ O₃ N⁷⁹ Br 603.8289 found 603.3304.

and

N-n-butyl, N-methyl-11-(16'α-bromo-3',17'β-dihydroxy-estra-1',3',5'(10')-trien-7α-yl)undecanamide ("EM 105")

(170 mg, 50%) as a colorless oil: analytical sample was obtained by HPLC purification: ¹ H-NMR δ(CDCl₃, 400 MHz), 0.80 (s,3H,18,--CH₃), 0.93 and 0.96 (2t,3H,J=7.3 Hz,N(CH₂)₃ CH₃), 2.80 (2H,J₆,6 =16.4,J₆,7 =4.6 Hz, Δδ=24.34 Hz, system ABX, 6'-H), 2.94 and 2.99 (2s,3H,N--CH₃), 3.27 (dd, 2H,J₁ =7.7 Hz and J₂ =7.5 Hz, --N--CH₂ --), 3.31-3.45 (m,2H,--N--CH₂ --), 4.02 (dd,1H,J₁₇,17 =3.7 Hz, and J₁₇,16 =6.1 Hz, 17'α-H), 4.15 (ddd,1H,J₁₆,15 =10.2 Hz, J₁₆,17 =6.1 Hz and J₁₆,15 =2.9 Hz, 16'β-H), 6.61 (d,1H,J=2.5 Hz, 4'-H), 6.66 (dd,1H,J=8.4 Hz and J₂ 2.5 Hz, 2'-H), 7.12 (d,1H,J=8.4 Hz, 1'-H,); IR ν_(max) (neat) 3320, 1610, 1490 cm⁻¹ ; MS m/e 605,603 (M⁺, 29%), 523 (M⁺ -HBr, 100%), 142 (C₂ H₄ CON(CH₃)C₄ H₉ ⁺, 70%), 114 (C₄ H₉ (CH₃)NCO⁺, 60%); Exact mass calculated for C₃₄ H₅₄ O₃ N⁷⁹ Br 603.3289, found 603.3289.

N-butyl, N-methyl-11-(16'α-iodo-3',17'β-dihydroxy-estra-1',3',5'(10')-trien-7'α-yl)undecanamide ("EM 156")

Under argon atmosphere, a mixture of 16α-bromodiol EM 105 (55 mg, 0.091 mmol) and dry sodium iodide (136 mg, 0.91 mmol) in freshly ethyl methyl ketone (25 ml) was refluxed in darkness during 12 h. Afterwards, the solvent was evaporated, water was added and the product was extracted with ethyl acetate. The organic phase was washed with 5% sodium thiosulfate and with water, dried over anhydrous sodium sulfate and concentrated to dryness under reduced pressure. The residue was purified by chromatography. Elution with a mixture of hexane-ethyl acetate (1:1, v/v) gave a mixture of starting material and iodo compound (52:48) of which HPLC separation afforded N-butyl, N-methyl-11,(16'-α-iodo-3',17'β-dihydroxy-estra-1',3',5'(10')-trien-7'α-yl )undecanamide ("EM 156") (21 mg, 36%) as colorless oil; ¹ H-NMR δ(CDCl₃, 400 MHz) 0.78 (s,3H,18'-CH₃), 0.93 and 0.96 (2t,3H,J=7.3 Hz, N(CH₂)₃ CH₃), 2.79 (2H,J₆,6 =16.5 Hz, J₆,7 =4.4 Hz,Δδ, =24.34 Hz, system ABX, 6'-H). 2.94 and 2.99 (2s,3H,N--CH₃), 3.27 (dd,2H,J₁ =7.6 Hz and J₂ =7.5 Hz, --N--CH₂) 3.32-3.44 (m, 2H N--CH₂), 4.09-4.17 (m, 2H, 16'βH and 17α-H), 6.60 (d,1H,J=2.4 Hz, 4'-H), 6.65 (dd,1H,J=8.4 Hz and J₂ =2.4 Hz, 2'-H), 7.13 (d,1H,J=8.4 Hz, 1'-H,); IR ν (neat) 3310, 1610, 1490 cm⁻¹ ; MS m/e 651 (M⁺,8%), 523 (M⁺ -HI, 100%), 508 (M⁺ -HI--CH₃,38%) 142 (C₂ H₄ CON(CH₃)C₄ H₉ ⁺, 54%), 114 (C₄ H₉ (CH₃)NCO⁺, 49%); Exact mass calculated for C₃₄ H₅₄ O₃ NI--HI 523.4028, found 523.4028.

Efficacy of an antiestrogen synthesized in accordance with Example 1

Compound "EM 139" shown in Scheme 2 above is an estrogen activity inhibitor. "EM 139" has been tested both for efficacy in acting as an antiestrogen by blocking estrogen receptors without substantially activating those receptors, and for efficacy in inhibiting 17β-hydroxysteroid dehydrogenase, an enzyme which catalyzes reactions involved in the synthesis of both androgens and estrogens (hereinafter referred to as "17β-HSD").

The antiestrogenic activity of "EM 139" was measured as its ability to inhibit the estradiol-induced stimulation of uterine weight in adult female ovariectomized Balb/c mice (body weight=19-20 g) sacrificed five days after ovariectomy. "EM 139", estradiol dissolved in ethanol were injected subcutaneously in the appropriate groups in a solution of 0.9% (w/v) sodium chloride and 1% (w/v) gelatin at different concentrations of "EM 139" (as noted along the X axis of FIG. 1.) A dosage of 0.2 ml of the foregoing preparation, was administered twice daily, starting on the day of ovariectomy for a total of 9 injections. Estradiol was injected at the dose of 0.01 μg in 0.2 ml, twice daily, starting on the morning after ovariectomy for a total of 8 injections.

After sacrifice, the uteri were rapidly removed, freed from fat and connective tissue and weighed. Results shown in FIG. 1 are the means ±SEM of groups of 9-10 mice. As may be seen from FIG. 1, EM 139 was highly potent to reduce estradiol-induced uterine weight gain.

To test the effect of "EM 139" on the inhibition of sex steroid formation, its effect on the 17β-hydroxysteroid dehydrogenase catalyzed conversion of estradiol to estrone was observed. The reaction was followed by monitoring formation of NADH (at 340 nm). The rate of conversion of cofactor NAD to NADH varies directly with the rate of estradiol conversion to estrone. The ability of "EM 139" to inhibit estrone production is indicative of its ability to inhibit the estrogen forming reverse reaction because both reactions are catalyzed by 17β-hydroxysteroid dehydrogenase (Thomas et al. J. Biol. Chem. 258: 11500-11504, 1983). 17β-hydroxysteroid dehydrogenase (17β-HSD) was purified to homogeneity from human placenta. A reaction vessel was prepared containing 1 μg 17β-HSD, 5 mM NAD, 20 μM 17β-estradiol, and the concentrations of the test compound "EM 139" which are indicated along the X-axis of FIG. 2 in 1.0 ml of a mixture of Tris-HCl (50 mM), EDTA (2 mM), MaN₃ (5 mM). The pH was 7.5. The reaction was allowed to proceed at 25° C. for 15 min. Formation of NADH was measured at 340 nm. As shown by FIG. 2, increasing concentrations of EM 139 significantly inhibited the reaction.

EXAMPLE 2

N-n-BUTYL, N-METHYL-11-(3',17'β-DIHYDROXY-17'α-ETHINYL-ESTRA-(1,',3',5'(10'),15'-TETRAEN-7'α-YL) UNDECANAMIDE ("EM 123") (Scheme 3)

N-n-butyl, N-methyl-11-(3'-benzoyloxy-17'-ethylenedioxy estra-1',3',5'(10')-,trien-7'α-yl)undecanamide (12)

A mixture of N-n-butyl, N-methyl-11-(3'-benzoyloxy-17'-oxo estra-1',3',5'(10')-trien-7'-α-yl)undecanamide (9a) (3.63 g), ethylene glycol (215 ml), p-toluenesulfonic acid (530 mg) and anhydrous benzene (250 ml) was refluxed with a Dean-Stark apparatus during 24 h. After cooling, the mixture was poured in water and extracted three times with ether. The organic layer was washed with a saturated sodium bicarbonate solution, and brine (3×), dried on magnesium sulfate and evaporated to dryness. The residue was purified by flash chromatography on silica-gel (Kieselgel 60, Merck, 230 mesh ASTM, 300 g). Elution with a mixture of hexane-ethyl acetate (6:4 v/v) gave pure N-butyl, N-methyl-11-(3'-benzoyloxyo-17'-ethylenedioxy estra-1',3',5'(10'), trien-7'α-yl)undecanamide (3.58 g, 92%) as an oil, the structure of which was confirmed by spectroscopic means.

N-n-butyl, N-methyl-11-(3'-benzoyloxy-16'α-bromo-17'α-ethylenedioxy-estra-1',3',5'(10'),trien-7'α-yl)undecanamide (13)

To the above ethylenedioxy amide 12 (370 mg, 0.55 mmol) in anhydrous tetrahydrofuran (10 ml) cooled at 0° C. was added dropwise under argon, a solution of pyridinium bromide perbromide (406 mg, 1.36 mmol) in 7 ml of the same solvent. After stirring during 1.5 h at 0° C., sodium iodide (300 mg) was added and the solution was stirred for 25 min. Afterwards, a solution of sodium thiosulfate (10%, v/v, 10 ml) and pyridine (0.5 ml) was added and the mixture was stirred for an additional 4 h and then poured into water and extracted three times with ether. The organic layers were washed with 1N hydrochloric acid, water, saturated bicarbonate solution and water (3×), dried on magnesium sulfate and evaporated to dryness. The residue was chromatographed on silica-gel (50 g). Elution with a mixture of hexane-ethyl acetate (4:1 v/v) gave pure N-n-butyl, N-methyl-11-(3'-benzoyloxy-16'α-bromo-17'-ethylenedioxy-estra-1',3',5'(10'),trien-7'α-yl)undecanamide (13) (313 mg, 76%) as colorless oil; IR ν_(max) (neat), 1730, 163 1595 and 1255 cm⁻¹ ; ¹ H NMR, 0.93 (3H, s, 18'-CH₃), 2.28 (2H, td, J=7.5 and 2.6 Hz, --CH₂ CON--), 2.90 and 2.95 (3H, 2s, --N--CH₃), 3.24 and 3.35 (2H, 2t, J=7.3 Hz, --N--CH₂ --), 3.85 and 4.35 (4H, m, --OCH₂ CH₂ O--), 4.56 (1H, m, H--C.16'), 6.91 (1H, d, J=2.2 Hz, H--C.4'), 6.98 (1H, dd, J=8.4 and 2.2 Hz, H--C.2'), 7.32 (1H, d, J=8.4 Hz, H--C.1'), 7.49 (2H, t_(app)., J=7.0 Hz H--C.3" and H--C.5"), 7.63 (1H, t_(app)., J=7.0 Hz, H--C.4") and 8.17 (2H, d, J=7.0 Hz, H--C.2" and H--C.6"), MS m/e, 671 (M⁺ -Br,11%), 114 (C₄ H₉ (CH₃)NCO⁺,13%), 105 (C₆ H₅ CO⁺,100%), 86 (C₄ H₉ (CH₃)N⁺,10%), 77 (C₆ H₅,25%).

N-n-butyl, N-methyl-11-(3'-hydroxy-17'-oxo-estra-1',3',5'(10'),15'-tetraen-7'α-yl)undecanamide "(EM 112)"

To a solution of the bromoketal (13) (517 mg, 0.69mmol) in anhydrous dimethyl sulfoxide warmed at 73° C., under argon, was added potassium-t-butoxide (1.55 g, 13.8mmol). The mixture was stirred for 5 h at this temperature and then cooled, poured in ice-water, acidified with 1N hydro-chloric acid and extracted three times with ethyl acetate. The organic layers were washed with water (3×), dried on magnesium sulfate and evaporated to dryness. The residue was dissolved in acetone (30 ml), water (7 ml) and p-toluenesulfonic acid (60 mg) was added. The resulting solution was stirred for 5 h at room temperature and then poured into water. The organic compound was extracted three times with ether, washed with a saturated sodium bicarbonate solution and water (3×), dried on magnesium sulfate and evaporated to dryness. The residue was purified by "flash chromatography" (100 g). Elution with a mixture of hexane-ethyl acetate (1:1 v/v) gave the pure N-butyl, N-methyl-11-(3'-hydroxy-17'-oxo-estra-1',3',5'(10'),15'-tetraen-7'α-yl)undecanamide "EM 112" (178 mg, 49%) as colorless oil; IR ν_(max) (neat), 3290, 1695, 1620 and 1600 cm⁻¹ ; ¹ H NMR, 0.92 and 0.95 (3H, 2t, J=7.3 and 7.0 Hz, --N--(CH₂)₃ CH₃), 1.11 (3H, s, 18'-CH₃), 2.32 (2H, td, J=2.5 and 7.0 Hz, H--C.2), 2.94 and 2.99 (3H, 2s, N--CH₃), 3.27 and 3.38 (2H, 2t, J=7.7 and 7.3 Hz, --N--CH₂ --), 6.11 (1H, dd, J=6.2 and 3.3 Hz, H--C.15'), 6.66 (1H, d, J=2.6 Hz, H--C.4'), 6.71 (1H, dd, J=8.4 and 2.6 Hz, H--C.2'), 7.13 (1H, d, J=8.4 Hz, H--C.1'), 7.60 (1H, dd, J=6.2 and 1.5 Hz, H--C.16') and 7.70 (1H, broad s, w_(1/2) =16 Hz, OH), MS m/e, 521 (M⁺,53%), 507 (M⁺ -CH₂,9%), 506 (M⁺ -CH₃,7%), 142 (C₂ H₄ CON(CH₃)C₄ H₉ ⁺,25%), 114 (C₄ H₉ (CH₃)NCO⁺,60%) and 86 (C₄ H₉ (CH₃)N⁺,22%), 44 (100%).

N-n-butyl, N-methyl-11-(3',17'β-dihydroxy-17'α-ethinyl-estra-1',3',5'(10'),15'-tetraen-7'α-yl)undecanamide ("EM 123")

To hexanes (1 ml) cooled at 0° C., were added trimethylsilylacetylene (0.112 ml), n-butyllithium 1.6M in hexanes (0.25 ml), few drops of anhydrous THF and finally, a slowly addition of a solution of enone amide EM 112 (57 mg) in anhydrous THF (1.2 ml). The mixture was stirred for 30 min at 0° C. After addition of a saturated ammonium chloride solution, the mixture was extracted with ethyl acetate (3×). The organic layers were washed with water and brine, dried over magnesium sulfate and filtered. The solvent was removed under reduced pressure. To the residue (61 mg) dissolved in methanol, a 5N potassium hydroxide solution (0.177 ml) was added and the mixture refluxed for 50 min. After cooling and addition of a saturated ammonium chloride solution, the mixture was extracted three times with ethyl acetate. The organic layers were washed with brine, dried over magnesium sulfate and filtered. The organic solvent was removed under reduced pressure. The residue was chromatographied on silica-gel (5 g). Elution with a mixture of hexanes:ethyl acetate (7:3 v/v) gave N-butyl, N-methyl-11-(3',17'β-dihydroxy-17'α-ethinyl-estra-1',3',5'(10'),15'-tetraen-7'α-yl)undecanamide ("EM 123") (34 mg, 63%); IR ν_(max) (neat), 3290, 2150, 1620 and 1600 cm⁻¹ ; ¹ H NMR, 0.92 and 0.95 (3H, 2t, J=7.3 and 7.0 Hz, N--(CH₂)₃ CH₃), 0.95 (3H, s, 18'-CH₃), 2.32 (2H, td, J=7.0 and 2 Hz, --CH₂ CON--), 2.66 (1H, s, --CH), 2.93 and 2.98 (3H, 2s, N--CH₃), 3.27 and 3.38 (2H, t, J=7.0 Hz, --N--CH₂ --), 5.78 (1H, dd, J=5.9 and 3.3 Hz, H--C.15'), 6.05 (1H, dd, J=5.9 and 1.5 Hz, H--C.16'), 6.62 (1H, d, J=2.5 Hz, H--C.4'), 6.67 (1H, dd, J=8.4 and 2.6 Hz, H--C.2') and 7.13 (1H, d, J=8.4 Hz, H--C.1') ppm; MS m/e 547 (M⁺,12%), 142 (C₂ H₄ CON(CH₃)C₄ H₉ ⁺,21%) 114 (C₄ H₉ (CH₃)NCO⁺,50%), 88 (100%) and 86 (C₄ H₉ (CH₃)N⁺,34%).

EXAMPLE 3 16β-Cyclopropyl Deravitives

N-n-butyl, N-methyl-11-(17'-oxo-3'-hydroxy-15'β,16'β-methylene-estra 1',3',5'(10')-trien-7'α-yl)undecanamide (14)

A solution of the phenol-enone EM 112 (101 mg; 0.19 mmol) dissolved in anhydrous pyridine (15 ml) and acetic anhydride (10 ml) was stirred at room temperature for 20 h. The mixture was into ice-water, then extracted three times with ether. The organic layers were washed with 1N hydrochloric acid, water and a saturated sodium bicarbonate solution and water, dried on magnesium sulfate and evaporated to dryness. The residue was purified by "flash chromatography" on silica-gel (20 g). Elution with a mixture of hexane-ethyl acetate (7:3 v/v) gave the N-butyl, N-methyl-11-(17'-oxo-3'-acetoxy-estra-1',3',5'(10'),15'-tetraen-7'α-yl)undecanamide.

To this and palladium (II) acetate (11 mg) in ether (25 ml) an ethereal diazomethane solution (prepared from 1 g of diazald) was added dropwise at 0° C. with continuous stirring during 10 min. After evaporation, the residue was dissolved in methanol (50 ml) and cooled to 0° C. 2N sodium hydroxide solution (1 ml) was added and after 75 min. of stirring the mixture was neutralized with 1N hydrochloric acid, extracted three times with ether. The organic layers were washed with brine, dried on magnesium sulfate and evaporated to dryness. The residue was purified by HPLC to give N-butyl, N-methyl-11-(17'-oxo-3'-hydroxy-15'β,16'β-methylene-estra-1',3',5'(10')-trien-7'α-yl)undecanamide (14) (79 mg, 76%) as a colorless oil. IR ν_(max) (neat) 3260, 1705, 1610 and 1570 cm⁻¹ ; ¹ H NMR (400 MHz) 0.93 and 0.96 (3H, 2t, J=7.3 Hz, N(CH₂)₃ CH₃), 0.99 (3H, s, 18'-CH₃), 1.98 (1H, td, J=8.3 and 3.96 Hz, H--C.16'), 2.80 (1H, d, J=16.6 Hz, Hβ--C.6'), 2.94 and 2.98 (3H, 2s, N--CH₃), 3.27 (1H, dd, J=7.58 and 6.66 Hz) and 3.38 (1H, m) (both are --N--CH₂ --), 6.64 (1H, d, J=2.6 Hz, H--C.4'), 6.66 (1H, dd, J=8.2 and 2.6 Hz, H--C.3') and 7.10 (1H, d, J=8.2 Hz, H--C.1') ppm; MS m/e 535 (M⁺,74%), 522 (M⁺ -CH₂,49%), 129 (C₄ H₉ (CH₃)NCOCH₃ ⁺,37%), 114 (C₄ H₉ (CH₃)NCO⁺,67%) and 88 (100%).

N-n-butyl, N-methyl-11-(3',17'β-dihydroxy-15'β,16'β-methylene-estra-1',3'5'(10')-trien-7'α-yl)undecanamide ("EM 136")

To the cyclopropylketone 14 (10 mg, 18.7 μmol) dissolved in methanol (8 ml) was added sodium borohydride (1.5 mg). The mixture was stirred at room temperature for 18 h. After addition of water, the mixture was concentrated under reduced pressure. The residue was diluted with water and extracted three times with ethylacetate. The organic layers were washed with brine, dried over magnesium sulfate and filtered. The organic solvent was removed under reduced pressure and the residue was purified by "flash chromatography" on silica-gel (5 g). Elution with a mixture of hexanes:ethyl acetate (5:5 v/v) gave N-butyl, N-methyl-11-(3',17'β-dihydroxy 15'β,16'β-cyclopropyl-estra-1',3',5'(10')-trien-7'α-yl)undecanamide ("EM 136"), as a colorless oil; IR ν_(max) (neat) 3300, 1615, 1580 and 1450 cm⁻¹, ¹ H NMR (400 HHz), 0.31 (1H, dd, J=14.0 and 7.8 Hz, H--C.1") 0.83 (3H, s, 18'-CH₃), 0.93 and 0.96 (3H, 2t, J=7.3 Hz, N(CH₂)₃ CH₃), 2.77 (1H, d, J=17.1 Hz, Hβ--C.6'), 2.94 and 2.98 (3H, 2s, N--CH₃), 3.27 (1H, dd, J=7.7 and 7.5 Hz) and 3.39 (1H, m) (both are --N--CH₂ --), 4.09 (1H, broad s, w=10 Hz, H--C.17'), 6.64 (2H, m, H--C.4' and H--C.2') and 7.11 (1H, d, J=8.3 Hz, H--C.1') ppm; MS m/e 537 (M⁺,18%), 5 19 (M⁺ -H₂ O,56%), 504 (M⁺ -H₂ O--CH₃,100%), 142 (C₂ H₄ CON(CH₃)C₄ H₉ ⁺,70%), 114 (C₄ H₉ (CH₃)NCO⁺,50%) and 86 (C₄ H₉ (CH₃)N⁺, 33%).

N-n-butyl, N-methyl-11-(3',17'β-dihydroxy-17'α-ethinyl-15'β,16'β-methylene-estra-1',3',5'(10')-trien-7'α-yl)undecanamide ("EM 138")

To hexanes (500 μl) cooled at 0° C., were added trimethylsilylacetylene (54.6 μl), 1.6M n-butyl lithium in hexanes (120.4 μl), few drops of anhydrous THF and finally, a slowly addition of a solution of the cyclopropyl ketone "EM 136" (25.8 mg) in anhydrous THF (350 μl). The mixture was stirred for 75 min at 0° C. After addition of a saturated ammonium chlorid solution (1 ml), the mixture was extracted three times with ethyl acetate. The organic layers were washed with water and brine, dried over magnesium sulfate and filtered. The solvent was removed under reduced pressure. To the residue dissolved in methanol (900 μl), a 5N potassium hydroxide solution (70 μl) was added and the mixture refluxed for 30 min. After cooling and addition of a saturated ammonium chloride solution (1 ml), the mixture was extracted three times with ethyl acetate. The organic layers were with washed with brine, dried over magnesium sulfate and filtered. The organic solvent was removed under reduced pressure. The residue was purified by "flash chromatography" on silica-gel (5 g). Elution with a mixture of hexanes:ethyl acetate (5:5 v/v) gave N-butyl, N-methyl-11-(3',17'β-dihydroxy-17'α-ethinyl-15'β,16'β-cyclopropyl-estra-1',3',5'(10')-trien-7'α-yl)undecanamide ("EM 138") (12 mg, 44%) as a colorless oil; IR ν_(max) (neat) 3590, 3300, 1620, 1600 and 1450 cm⁻¹ ; ¹ HNMR (400 MHz), 0.39 (1H, ddd, J=14.6 and 7.9 Hz, H--C.1'), 0.93 and 0.96 (3H, 2t, J=7.4 and 7.3 Hz, --N(CH₂)₃ --CH₃), 0.96 (3H, s, 18'-CH₃), 2.70 (1H, s, --C CH), 2.77 (1H, d, J=16.5 Hz, Hβ--C.6'), 2.94 and 2.98 (3H, s, N--CH₃), 3.27 (1H, dd, J=7.7 and 7.6 Hz) and 3.38 (1H, m) (both are N--CH₂ --), 6.42 (1H, m, OH), 6.65 (2H, m, H--C.4' and H--C.2') and 7.12 (1H, d, J=8.3 Hz, H--C.1') ppm; MS m/e 561 (M⁺,15%), 142 (C₂ H₄ CON(CH₃)C₄ H₉ ⁺,66%), 114 (C₄ H₉ (CH₃)CO⁺,53%), 88 (100%) an 86 (C₄ H₉ (CH₃)N⁺,35%). ##STR20##

17α-ALKYNYLAMIDE ESTRADIOLS

General Procedure for Ester Formation (scheme 4 A)

In anhydrous conditions under argon atmosphere, bromo acid (17 mmol) was dissolved in dry CH₂ Cl₂ (30 ml), oxalyl chloride (12 ml) was added and the reaction was stirred 2 h at room temperature. Then, dry benzene was added to mixture and solvent was evaporated under reduced pressure (2×) and dried under vacuum. This crude product was dissolved in dry CH₂ Cl₂ (20 ml) and added at 0° C. to a solution of 3-methyl 3-oxetanemethanol (17 mmol), CH₂ Cl₂ (7 ml) and pyridine (1.4 ml). The reaction was keeped at this temperature for 4-8 h. Thereafter, mixture was diluted with CH₂ Cl₂, washed with NaHCO₃ (10%, w/v) and organic phase was dried over MgSO₄. After removal of solvent, residue was purified by chromatography (hexane-ethylacetate-triethylamine/80:20:1, v/v/v) to afford bromo ester.

6-bromo hexanoate ester of 3-methyl-3-hydroxymethyloxetane (15).

Light yellow liquid (91% yield); IR ν (neat) 2930, 2860, 1725, 1450, 1370, 1160 cm⁻¹ ; NMR-60 δ(CDCl₃) 1.31 (s, 3H), 1.1-2.1 (m, 6H), 2.36 (t, J=6.0 Hz, 2H), 3.36 (t, J=6 Hz, 2H), 4.13 (s, 2H), 4.41 (AB system Δν=8.3, J=6 Hz, 4H).

9-bromo nonanoate ester of 3-methyl-3-hydroxymethyloxetane (16).

Colorless liquid (86% yield); IR ν (neat) 2920, 2840, 1725, 1450, 1370, 1150 cm⁻¹ ; NMR-60 δ(CDCl₃) 1.31 (s, 11H), 1.2-2.2 (m, 4H), 2.40 (t, J=6.0 Hz, 2H), 3.45 (t, J=6.0 Hz, 2H), 4.20 (s, 2H), 4.48 (AB system Δν=8.2, J=6.0 Hz, 4H).

11-bromo undecanoate ester of 3-methyl-3-hydroxymethyl oxetane (17).

Colorless liquid (85% yield); NMR-60 δ(CDCl₃) 1.33 (s, 15H), 1.0-2.0 (m, 4H), 2.30 (t, J=6.0 Hz, 2H), 3.35 (t, J=6.0 Hz, 2H), 4.12 (s, 2H), 4.40 (AB system Δν=8.2, J=6.0 Hz, 4H).

12-bromo dodecanoate ester of 3-methyl-3-hydroxymethyl oxetane (18).

Colorless liquid (86% yield); IR ν (neat) 2910, 2840, 1720, 1450, 1370, 1155 cm⁻¹ ; NMR-60 δ(CDCl₃) 1.30 (s, 17H), 1.1-2.0 (m, 4H), 2.30 (t,J=6.0 Hz, 2H), 3.33 (t, J=6.0 Hz, 2H), 4.11 (s, 2H), 4.40 (AB system Δν=8.0, J=6.0 Hz, 4H).

General Procedure for Ortho Ester Formation (scheme 4A)

To a solution of bromo ester (3.4-14.2 mmol) in dry CH₂ Cl₂ (10-40 ml) at 0° C. was added with stirring distilled boron trifluoride etherate (0.85-3.55 mmol). After 4 h at 0° C., reaction mixture was quenched by the addition of triethylamine (3.4-14.2 mmol), diluted with diethylether and filtered to remove the amine-BF₃ complex. The filtrate was evaporated and residue was purified by chromatography (hexane-ethylacetatetriethylamine/80:20:1, v/v/v) to give bromo ortho ester.

1-(5'-bromo pentanyl)-4-methyl-2,6,7-trioxabicyclo 2.2.2!octane 19.

Colorless oil (68% yield): IR ν (neat) 2940, 2915, 2855, 1450, 1390, 1050, 980 cm⁻¹ : NMR-60 δ(CDCl₃) 0.79 (s, 3H), 1.2-2.0 (m, 8H), 3.35 (t, J=6.0 Hz, 2H), 3.87 (s, 6H) MS m/e (rel. intensity) 280 (M⁺, 0.2), 278 (M⁺, 0.2), 250 (8.1), 248 (8.5), 197 (7.2), 195 (7.7), 179 (58), 177 (61), 72 (54), 69 (100).

1-(8'-bromo octanyl)-4-methyl-2,6,7-trioxabicyclo 2.2.2!octane (20).

Amorphous white solid (69% yield); IR ν (KBr) 2940, 2900, 2840, 1450, 1390, 1045, 985, 950 cm⁻¹ ; NMR-60 δ(CDCl₃) 0.80 (s, 3H), 1.33 (s, 8H), 1.0-2.1 (m, 6H), 3.40 (t, J=6.0 Hz, 2H), 3.93 (s, 6H); MS m/e (rel. intensity) 323 (M⁺, 2.1), 321 (M⁺, 2.0), 292 (4.4), 290 (5.1), 239 (8.6), 237 (7.1), 221 (34), 219 (33), 69 (71), 55 (100).

1-(10'-bromo decanyl)-4-methyl-2,6,7-trioxabicyclo 2.2.2!octane (21).

White solid (74% yield); m.p. 51°-53° C.; IR ν (KBr) 2940, 2900, 2850, 2830, 1455, 1390, 1055, 985, 955 cm⁻¹ ; NMR-60 δ(CDCl₃) 0.80 (s, 3H), 1.27 (s, 12H), 1.1-2.1 (m, 6H), 3.39 (t, J=6.0 Hz, 2H), 3.87 (s, 6H); MS m/e (rel. intensity) 350 (M⁺, 1.2), 348 (M⁺, 1.1), 321 (3.0), 319 (7.6), 269 (7.5), 248 (97), 144 (37), 55 (100).

1-(11'bromo undecananyl)-4-methyl-2,6,7-trioxabicyclo 2,2,2!octane (22).

White solid (76%, yield); m.p. 47.5, 48.5° C.; IR ν (KBr) 2900, 2835, 1460, 1045, 975 cm⁻¹ ; NMR-60 δ(CDCl₃) 0.79 (s, 3H), 1.25 (s, 14H), 1.1-2.1 (m, 6H), 3.37 (t, J=6.0 Hz, 2H), 3.85 (s, 6H); MS m/e (rel. intensity) 364 (M⁺, 3.5), 362 (M⁺, 3.4), 334 (13), 332 (13), 283 (15), 263 (85), 261 (97), 144 (51), 55 (100).

4. Preparation of 17α-aklynylamide estradiols (scheme 4B)

General Procedure for Coupling Reaction

In a flame-dried flask under argon atmosphere, 3,17β-bis tetrahydropyranyl ethinylestradiol 23 (1.5 mmol) synthesized from commercial ethynyl estradiol and dihydropyran was dissolved in dry THF (40 ml) and HMPA (6.0 mmol). The solution was cooled at -7820 C. and n-BuLi (3.0 mmol) was added. After 2 h, appropriate bromo ortho ester 19-22 (6.0 mmol) in dry THF (10 ml) was added at -78° C. The mixture was allowed to return slowly at room temperature and keeped at this temperature overnight. Then, brine was added and the reaction mixture was extracted with ethylacetate. The organic phase was dried over MgSO₄ and the solvent was removed under reduced pressure. The crude product was purified by chromatography (hexane-ethylacetate-triethylamine/96:4:1 to 50:50:1, v/v/v) to give coupling product 24-27, unreacted steroid 23 (61, 22, 57%) and small quantity of undeterminated product.

1-{3',17'β-bis (tetrahydro-2"H-pyran-2"yl)oxy!estra-1',3',5'(10')-trien-17'α-yl}-7-(4'-methyl-2',6',7'-trioxabicyclo 2'.2'.2'!octan-1'-yl)-1-heptyne (24).

Colorless oil (15% yield); IR ν (neat) 2920, 2855, 2230 w, 1600, 1485 cm⁻¹ ; NMR-60 δ(CDCl₃) 0.75 (s, 3H), 0.88 (s, 3H), 2.80 (m, 2H), 3.2-4.1 (m, 4H), 3.80 (s, 6H), 4.9-5.3 (m, 1H), 5.34 (s, 1H), 6.75 (m, 2H), 7.19 (d, J=8.0 Hz, 1H); MS m/e (rel. intensity) 579 (M⁺ -DHP, 4.0), 564 (1.1), 494 (12), 477 (12), 374 (13), 85 (100).

1-{3',17'β-bis (tetrahydro-2"H-pyran-2"yl)oxy!estra-1',3',5'(10')-trien-17'α-yl}-10-(4'methyl-2'.6'.7'-trioxabicyclo 2'.2'.2'!octan-1'-yl)-1-decyne (25).

Colorless oil (15% yield); IR ν (neat) 2915, 2850, 2210 w, 1600, 1485 cm⁻¹ ; NMR-200 δ(CDCl₃) 0.79 (s, 3H), 0.90 (s, 3H), 2.24 (t, J=6.6 Hz, 2H), 2.83 (m, 2H), 3.55 (m, 2H), 3.89 (s, 6H), 3.95 (m, 2H), 4.98 and 5.19 (2s, 1H), 5.39 (s, 1H), 6.78 (d, J=2.6 Hz, 1H), 6.84 (dd, J₁ =2.6 Hz and J₂ =8.4 Hz, 1H), 7.22 (d, J=8.4 Hz, 1H); MS m/e (rel. intensity) 620 (M⁺ -DHP, 4.8), 535 (13), 518 (8.9), 85 (100).

1-(3',17'α-bis (tetrahydro-2"H-pyran-2"yl)oxy!estra-1',3',5'(10')-trien-17'α-yl}-12-(4'methyl-2',6',7'-trioxabicyclo 2'.2'.2'!octan-1'-yl)-1-dodecyne (26).

Colorless visquous oil (42% yield); IR ν (neat) 2920, 2850, 2210 w, 1600, 1485 cm⁻¹ ; NMR-200 δ(CDCl₃) 0.79 (s, 3H), 0.90 (s, 3H), 2.25 (t, J=6.6 Hz, 2H), 2.83 (m, 2H), 3.55 (m, 2H), 3.89 (s, 6H), 3.95 (m, 2H), 5.0 and 5.2 (2s, 1H), 5.39 (s, 1H), 6.78 (d, J=2.6 Hz, 1H), 6.84 (dd, J₁ =2.6 Hz and J₂ =8.4 Hz, 1H), 7.21 (d, J=8.4 Hz, 1H); MS m/e (rel. intensity) 649 (M⁺ -DHP, 6.1), 634 (0.7), 564 (22), 547 (16), 85 (100).

1-{3'17'β-bis (tetrahydro-2"H-pyran-2"yl)oxy!estra-1'3'5'(10')-trien-17'α-yl}-13-(4'methyl-2',6',7'-trioxabicyclo 2'.2'.2'!octan-1'yl)-1-tride cyne (27).

Colorless visquous oil (35% yield); IR ν (neat) 2915, 2850, 2290 w, 1600, 1490 cm⁻¹ ; NMR-200 δ(CDCl₃) 0.80 (s, 3H), 0.90 (0.3H), 2.25 (t, J=6.6 Hz, 2H), 2.83 (m, 2H), 3.53 (m, 2H), 3.89 (s, 6H), 3.95 (m, 2H), 5.0 and 5.2 (2s, 1H), 5.39 (s, 1H), 6.78 (d, J=2.2 Hz, 1H), 6.84 (dd, J₁ =2.6 and J₂ =8.4 Hz, 1H), 7.21 (d, J=8.4 Hz, 1H).

General Procedure for Ortho Ester and di-THP Hydrolysis

The product with ortho ester and di-THP group (0.22-0.63 mmol) was dissolved in MeOH (80-120 ml) and p-toluenesulfonic acid (0.17-0.23 mmol) was added. The solution was stirred at room temperature for 2-3 h. Then, water was added, MeOH was removed under reduced pressure and residue was extracted with ethylacetate. After evaporation of solvent, the crude product was purified by column chromatography (hexane-ethylacetate/5:5, v/v) to give ester compound with free hydroxyl group.

8-(3',17'α-dihydroxy estra-1',3',5'(10')-trien-17'α-yl)-7-octynoate ester of 2',2'-dihydroxymethyl propanol (28).

Colorless visquous oil (70% yield); IR ν (film) 3340, 2910, 2850, 1710, 1600, 1485 cm⁻¹ ; NMR-200 δ(CDCl₃) 0.83 (s, 3H), 0.86 (s, 3H), 2.27 (t, J=6.4 Hz, 2H), 2.38 (t, J=7.1 Hz, 2H), 2.81 (m, 2H), 3.54 (s broad, 4H), 4.17 (s, 2H), 4.87 (s, 1H), 6.56 (d, J=2.6 Hz, 1H), 6.63 (dd, J₁ =2.6 Hz and J₂ =8.4 Hz, 1H), 7.17 (d, J=8.4 Hz, 1H); MS m/e (rel. intensity) 512 (M⁺,14), 494 (17), 479 (17), 466 (11), 270 (48), 159 (100).

11-(3',17'α-dihydroxy estra-1',3',5'(10')-trien-17'α-yl)-10-undecynoate ester of 2',2'-dihydroxymethyl propanol (29).

Colorless visquous oil (61% yield); IR ν (neat) 3360, 2910, 2840, 2210 vw, 1710, 1600, 1485 cm⁻¹ ; NMR-200 (CDCl₃) δ0.84 (s, 3H), 0.86 (s, 3H), 2.24 (t, J=7.0 Hz, 4H), 2.79 (m, 2H), 3.34 (s broad, 2H), 3.56 (s broad, 4H), 4.13 (s, 2H), 6.57 (s_(app), 1H), 6.63 (dd, J₁ =2.6 Hz and J₂ =8.4 Hz, 1H), 7.14 (d, J=8.4 Hz, 1H) MS m/e (rel. intensity) 554 (M⁺, 5.0), 536 (57), 520 (10), 507 (7.6), 435 (14), 419 (20), 270 (39), 160 (85), 133 (100).

13-(3',17'α-dihydroxy estra-1',3',5'(10')-trien-17'α-yl)-12-tridecynoate ester of 2',2'-dihydroxymethyl propanol (30).

Colorless visquous oil (78% yield); IR ν (film) 3360, 2915, 2840, 1710, 1600, 1490 cm⁻¹ ; NMR-200 δ(CDCl₃) 0.83 (s, 6H), 2.25 (m, 4H), 2.78 (m, 2H), 3.53 (s broad, 4H), 4.09 (s, 2H), 6.6 (m, 2H), 7.10 (d, J=8.0 Hz, 1H); MS m/e (rel. intensity) 582 (M⁺, 1.0), 563 (38), 548 (5.7), 535 (3.5), 463 (5.7), 446 (13), 270 (44), 160 (57), 133 (58), 55 (100).

14-(3',17'β-dihydroxy estra-1',3',5'(10')-trien-17'α-yl)-13-tetradecynoate ester of 2',2'-dihydroxymethyl propanol (31).

Colorless visquous oil (83%, yield); IR ν (film) 3360, 2910, 2840, 2220 vw, 1710, 1605, 1490 cm⁻¹ ; NMR-200 δ(CDCl₃) 0.85 (s, 3H), 0.87 (s, 3H), 2.25 (t, J=6.6 Hz, 2H), 2.33 (t, J=7.1 Hz, 2H), 2.80 (m, 2H), 2.9 (m, 2H), 3.58 (s broad, 4H), 4.20 (s, 2H), 5.72 (s, 1H), 6.56 (d, J=2.6 Hz, 1H), 6.62 (dd, J₁ =2.6 Hz and J₂ =8.4 Hz, 1H), 7.15 (d, J=8.8 Hz, 1H).

General Procedure for Hydrolysis of Ester Following by Amide Formation

At a solution of ester (0.14-0.49 mmol) in MeOH (12-50 ml) was added aqueous solution of KOH 10% w/v (6-25 ml) and mixture was refluxed under argon atmosphere for 24 h. Thereafter, water was added and MeOH was evaporated under reduced pressure. The resulting solution was acidified with HCl and extracted with ethylacetate. Organic phase was washed with water, brine and dried over MgSO₄. Without purification, the crude carboxylic acid (IR acid band at 1700 and 2400-3600 cm⁻¹) was dissolved in dry CH₂ Cl₂ (20-70 ml) and tributylamine (0.58-2.04 mmol). The mixture was cooled at -10° C., isobutyl chloroformate (0.68-2.41 mmol) was added and allowed to react 30 min. At this time, N-methylbutylamine in excess (4.2-16.0 mmol) was added and the cooling bath was removed. After 2 h, CH₂ Cl₂ was added and organic phase was washed with HCl (1N) and dried over MgSO₄. The solvent was removed and crude amide purified by column chromatography (hexane-ethylacetate/7:3, v/v).

N-butyl, N-methyl-8- 3'-(i-butyloxy carbonyloxy)-17'β-hydroxy estra-1',3',5'(10')-trien-17'α-yl!-7-octynamide (32).

Colorless oil (79% yield); IR ν (neat) 3380, 2920, 2850, 1745, 1620 cm⁻¹ ; NMR-200 δ(CDCl₃) 0.87 (s, 3H), 0.91 and 0.94 (2t, J=7.3 Hz, 3H), 1.00 (d, J=6.6 Hz, 6H), 2.85 (m, 2H), 2.89 and 2.91 (2s, 3H), 3.22 and 3.33 (2t, J=7.5 Hz, 2H), 4.02 (d, J=7.0 Hz, 2H), 6.88 (d, J=2.6 Hz, 1H), 6.93 (dd, J₁ =2.6 Hz and J₂ =8.4 Hz, 1H), 7.29 (d, J=8.4 Hz, 1H): MS m/e (rel. intensity) 579 (M⁺, 12), 561 (26), 546 (11), 461 (6.7), 447 (3.7), 270 (84), 57 (100). EMS M⁺ calculated for C₃₆ H₅₃ O₅ N: 579.3923; found: 79.3970.

N-butyl, N-methyl-11- 3'-(i-butyloxy carbonyloxy)-17'β-hydroxy estra-1',3',5'(10')-trien-17'α-yl!-10-undecynamide (33).

Colorless oil (67% yield); IR ν (neat) 3370, 2910, 2840, 1745, 1620 cm⁻¹ ; NMR-200 δ(CDCl₃) 0.87 (s, 3H), 0.92 and 0.95 (2t, J=6.6 Hz, 3H), 1.00 (d, J=7.0 Hz, 6H), 2.86 (m, 2H), 2.90 and 2.94 (2s, 3H), 3.24 and 3.35 (2t, J=7.3 Hz, 2H), 4.03 (d, J=6.6 Hz, 2H), 6.88 (d, J=2.6 Hz, 1H), 6.93 (dd, J₁ =2.6 Hz and J₂ =8.8 Hz, 1H), 7.30 (d, J=8.1 Hz, 1H); MS m/e (rel. intensity) 621 (M⁺, 2.1), 606 (2.4), 602 (6.2), 212 (43), 159 (69), 142 (68), 114 (100).

N-butyl, N-methyl-13- 3'(i-butyloxy carbonyloxy)-17'β-hydroxy estra-1',3',5'(10')-trien-17'α-yl!-12-tridecynamide (34).

Colorless oil (89% yield); IR ν (neat) 3370, 2920, 2840, 1745, 1620 cm⁻¹ ; NMR-200 δ(CDCl₃) 0.87 (s, 3H), 0.92 and 0.95 (2t, J=7.0 Hz, 3H), 1.00 (d, J=7.0 Hz, 6H), 2.86 (m, 2H), 2.90 and 2.96 (2s, 3H), 3.25 and 3.35 (2t, J=7.4 Hz, 2H), 4.02 (d, J=6.6 Hz, 2H), 6.88 (d, J=2.2 Hz, 1H), 6.93 (dd, J₁ =2.6 Hz and J₂ =8.4 Hz, 1H), 7.30 (d, J=8.8 Hz, 1H); MS m/e (rel. intensity) 649 (M⁺, 20), 633 (15), 631 (18), 616 (8.2), 531 (15), 516 (5.6), 270 (85), 57 (100); EMS M⁺ calculated for C₄₁ H₆₃ O₅ N: 649.4706 found: 649.4643.

N-butyl, N-methyl-14- 3'(i-butyloxy carbonyloxy)-17'β-hydroxy estra-1',3'5'(10')-trien-17'α-yl!-13-tetradecynamide (35).

Colorless oil (83%, yield); IR ν (neat) 3380, 2910, 2840, 1750, 1625 cm⁻¹ ; NMR-200 δ(CDCl₃) 0.87 (s, 3H), 0.92 and 0.95 (2t, J=7.0 Hz, 3H), 1.00 (d, J=6.6 Hz, 6H), 2.85 (m, 2H), 2.91 and 2.96 (2s, 3H), 3.25 and 3.36 (2t, J=7.4 Hz, 2H), 4.03 (d, J=6.6 Hz, 2H), 6.88 (d, J=2.6 Hz, 1H), 6.93 (dd, J₁ =2.9 Hz and J₂ =8.4 Hz, 1H), 7.30 (d, J=8.8 Hz, 1H); MS m/e (rel. intensity).

Hydrolysis of Carbonate

Hydrolysis of carbonate compounds 32-35 was performed as follows: carbonate derivatives were dissolved in methanol (10 ml) K₂ CO₃ (1%; p/v) in aqueous methanol (25:75, v/v) (10 ml) was added and the resulting solution was stirred at room temperature for 3 h. Reaction mixture was acidified with HCl (1N) and MeOH was evaporated under vacuum. The residue was extracted with ethyl acetate and organic phase was dried, evaporated and purified by column chromatography (hexane-ethylacetate) 6.5:3.5, v/v).

N-butyl, N-methyl-8- 3',17'β-dihydroxy estra-1',3',5'(10')-trien-17'α-yl!-7-octynamide ("EM 157").

Purified by column chromatography (hexane-ethylacetate/4:6, v/v). Amorphous white solid (881 yield); IR ν (film) 3280, 2910, 2840, 1610 cm⁻¹ ; NMR-200 δ(CDCl₃) 0.87 (s, 3H), 0.91 and 0.94 (2t, J=7.0 Hz, 3H), 2.80 (m, 2H), 2.90 and 2.92 (2s, 3H), 3.22 and 3.34 (2t, J=7.3 Hz, 3H), 5.22 (s, 1H), 6.57 (d, J=2.9 Hz, 1H), 6.64 (dd, J₁ =2.6 Hz and J₂ =8.4 Hz, 1H), 7.16 (d, J=8.4 Hz, 1H); MS m/e (rel. intensity) 479 (M⁺, 11), 462 (18), 460 (38), 446 (18), 270 (30), 114 (56), 88 (67), 44 (100); EMS M⁺ calculated for C₃₁ H₄₅ O₃ N: 79.3399; found: 479.3369.

N-butyl, N-methyl-11- 3',17'β-dihydroxy estra-1',3',5'(10')-trien-17'α-yl)-10-undecynamide ("EM 183").

Purified by column chromatography (hexane-ethylacetate/4:6, v/v). Amorphous white solid (83% yield); IR ν (KBr) 3300, 2910, 2840, 1610 cm⁻¹ ; NMR-200 δ(CDCl₃) 0.87 (s, 3H), 0.93 and 0.95 (2t, J=7.0 Hz, 3H), 2.80 (m, 2H), 2.91 and 2.94 (2s, 3H), 3.23 and 3.35 (2t, J=7.3 Hz, 2H), 5.30 (s, 1H), 6.57 (d, J=2.6 Hz, 1H), 6.64 (dd, J₁ =2.6 Hz and J₂ =8.4 Hz, 1H), 7.16 (d, J=8.1 Hz, 1H); MS m/e (rel. intensity) 521 (M⁺, 4.4), 505 (10), 502 (26), 489 (7.7), 487 (8.7), 270 (20), 114 (55), 88 (42), 44 (100).

N-butyl, N-methyl-13- 3',17'β-dihydroxy estra-1',3',5'(10')-trien-17'α-yl!-12-tridecynamide ("EM 163").

Purified by column chromatography (hexane-ethylacetate/7:3, v/v). Amorphous white solid (98% yield); IR ν (film) 3300, 2910, 2840, 1610 cm⁻¹ ; NMR-200 δ(CDCl₃) 0.88 (s, 3H), 0.93 and 0.95 (2t, J=7.0 Hz, 3H), 2.80 (m, 2H), 2.93 and 2.97 (2s, 3H), 3.25 and 3.38 (2t, J=7.5 Hz, 2H), 6.61 (d, J=2.6 Hz, 1H), 6.69 (dd, J₁ =2.6 Hz and J₂ =8.6 Hz, 1H), 6.87 (s, 1H), 7.14 (d, J=8.1 Hz, 1H); MS m/e (rel. intensity) 549 (M⁺, 8.7), 532 (17), 530 (23), 516 (12), 270 (30), 114 (35), 88 (45), 44 (100); EMS M⁺ calculated for C₃₆ H₅₅ O₃ N: 549.4182, found: 549.4271.

N-butyl, N-methyl-14- 3',17'α-dihydroxy estra-1',3',5'(10')-trien-17'α-yl!-13-tetradecynamide ("EM 196").

Purified by column chromatography (hexane-ethylacetate/6:4, v/v). Amorphous white solid (93% yield); IR ν (film) 3280, 2915, 2840, 1615 cm⁻¹ ; NMR-200 δ(CDCl₃) 0.88 (s, 3H), 0.94 and 0.95 (2t, J=7.0 Hz, 3H), 2.80 (m, 2H), 2.95 and 2.98 (2s, 3H), 3.26 and 3.39 (2t, J=7.3 Hz, 2H), 6.61 (d, J=2.2 Hz, 1H), 6.70 (dd, J₁ =2.6 Hz and J₂ =8.4 Hz, 1H), 7.13 (m, 2H: aromatic and phenolic hydrogen). ##STR21##

EXAMPLE 6

N-n-butyl, N-methyl-(3'-17'β-dihydroxy-11'β-methoxy estra 1',3',5'(10')-trien 7'α-yl)undecanamide ("EM 111") and its 17β-ethinyl derivatives ("EM 121"). ##STR22##

EXAMPLE 6A

11β-chloromethyl derivatives

N-N-butyl, n-methyl, (11β-chloromethyl-3',17'β-dihydroxy-estra-1',3',5(10')-trien-7'.alpha.-yl)undecanamide (56). and its 17α-ethinyl derivative (58). ##STR23##

EXAMPLE 7

Compounds with aliphatic side-chain in 17α-position

N-n-butyl, n-methyl, 17'β-hydroxy-3'-methoxy estra-1',3',5',(10')-trien-17α'α-yl)undecanamide ("EM 103"). ##STR24##

EXAMPLE 8

17α-cyclopropyl derivatives

N-n-butyl, N-methyl-(17'α-cyclopropyl-3',17β-dihydroxy estra-1',3',5',(10)-trien-7'α-yl)undecanamide (68) and its 17'α-chlorocyclopropyl and 17'α-fluorocyclopropyl derivative (69). ##STR25##

EXAMPLE 9

N-n-butyl, N-methyl-(17'α-cyclopropyl-3',17β-dihydroxy 11'β-methoxy estra 1',3',5',(10)-trien-7'α-yl) undecanamide (70 X═H) and its 17'α-chlorocylopropyl and 17'α-fluorocyclopropyl derivative (70, X═F, Cl).

Same example as Example-8 with compound 49 as starting material. ##STR26##

EXAMPLE 10

17α-cyanovinyl derivatives

N-n-butyl, N-methyl-(17'α-cyclopropyl-3',17β-dihydroxy 11'β-methoxy estra 1',3',5',(10)-trien-7'α-yl)undecanamide (73). ##STR27##

EXAMPLE 11

Compounds with aliphatic side chain in 15α-position

N-n-butyl, N-methyl-(3',17β-dihydroxy 17'α-ethinyl estra 1',3',5',(10)-trien-15'α-yl)undecanamide ("EM 108"). ##STR28##

EXAMPLE 12

17α-thioethyl derivatives

N-n-butyl, N-methyl-(3',17β-dihydroxy 17'α-thioethyl estra 1',3',5',(10)-trien-7'α-yl)undecanamide (82) and its ethyl disulfite derivative (83). ##STR29##

EXAMPLE 13

17α-thiopropyl derivatives

N-n-butyl, N-methyl-(3',17β-dihydroxy 17α-thiopropyl estra-1',3',5'-derivatives (10')-trien-7'α-yl)undecanamide (84) and its ethyl disulfite derivative (86). ##STR30##

EXAMPLE 14

11β-ethyl derivatives

N-n-butyl, N-methyl-(3',17β-dihydroxy 17'α-ethinoyl-11β-ethyl estra 1',3',5'(10')trien-7'α-yl)undecanamamide (97). ##STR31##

EXAMPLE 15

14,15 epoxide derivatives

N-n-butyl, N-methyl-(3',17p-dibenzoyl-14',15'-epoxy-estra 1',3',5'(10')trien-7'α-yl)undecanamide ("EM 180") and ("EM 181"). ##STR32##

EXAMPLE 16

N-n-butyl, N-methyl-11-(3',17'α-dihydroxy estra-1',3',5'(10')trien-7'α-yl)undecanamide ("EM 187") ##STR33##

EXAMPLE 17

N-n-butyl, N-methyl-11-(6'-hydroxy-2'-(4"-hydroxyphenyl )-3'-ethyl-indol-N'-yl)undecanamide (104).

The starting material 101 has been synthesized as described by Von Angerer et al., J. Med. Chem. 27: 1439-1447, 1984. ##STR34##

EXAMPLE 18

N-n-butyl, N-methyl-11-(6'-hydroxy-2'-(4"-hydroxyphenyl)-(1',2'-dehydronaphtalen-3'-yl)undecanamide (110). ##STR35##

EXAMPLE 19

N-n-butyl, N-methyl-11- 4,4'-(1,2-diethyl-1,2-ethanydyl) bis-phenol-3-yl)undecanamide (115) ##STR36##

Other sex steroid activity inhibitors in accordance with the inventions may be synthesized by methods known in the art, by methods analogous to those set forth above and by modifying the synthesis set forth above in a manner known in the art.

The terms and descriptions used here are preferred embodiment set-forth the way of illustration only and are not intended as limitations on the many variations which those of skill in the art will recognize to be possible in practicing the present invention as defined by the following claims. 

What is claimed is:
 1. A sex steroid activity inhibiting compound selected from the group consisting of: ##STR37##
 2. A sex steroid activity inhibiting compound selected from the group consisting of: ##STR38## wherein R³ and R¹⁷ are independently selected from the group consisting of H-- and ##STR39##
 3. A pharmaceutical composition comprising a pharmaceutically acceptable diluent or carrier and a therapeutically effective amount of sex steroid inhibiting compound of claim
 1. 4. A pharmaceutical composition comprising a pharmaceutically acceptable diluent or carrier and a therapeutically effective amount of sex steroid inhibiting compound of claim
 2. 5. A method for treating breast cancer in a human or other warm blooded patient in need of such treatment, said method comprising administering to said patient, with or without additional carrier or diluent, a therapeutically effective amount of the sex steroid activity inhibiting compound of claim
 1. 6. A method for treating breast cancer in a human or other warm blooded patient in need of such treatment, said method comprising administering to said patient, with or without additional carrier or diluent, a therapeutically effective amount of the sex steroid activity inhibiting compound of claim
 2. 